Regulatory training

COVALENT:- Covalent is a group of company which has services and operations in Clinical, Information Technology, Energy, consumer products, Power and Infrastructure. Training @ Covalent:- We arededicated to establish ourselves as ''A values-driven organization''. These values will continue to direct our growth and organization’s operation. “Covalent” values supporting the way like “Kreative”. Regulatory Affairs(RA) Training or Course:- Introduction to different types of Pharmaceutical products: Basic concepts on Rx, OTC, API, Starting material, DP/FP, Generics vs. Innovator drugs, Biologics vs. Biosimilars, Laws vs. Regulations vs. guidelines. Drug discovery and development Worldwide regulatory agencies and their role Approval process for each of the below products in US/EU/India: [covers development path, submissions, regulatory expectation for development, approval and market] Post-market regulatory obligations GLP’s: 21 CFR 58 -The History of GLP, The Idea behind GLP, The Areas of Application, The Pillars of Good Laboratory Practice, Where Can GLP be Profitably Applied?, Indian GLP and International GLP. CMC topics: GMP (US/EU/Indian/ PIC), Preformulation studies (Drugs and Generics), ICH Q 7 guideline, 21 CFR 210 and 211, Medical device CE marking and ISO certifications. Audits, pre and post approval Inspections, handling post inspection/ audit queries. Collecting, organizing and compiling various regulatory submissions in compliance with the applicable regulations: ASEAN and BRIC regulations and registration process of Drugs and Biologics. Different stages of interactions, briefing packages, responses and corrective measures during drug approval process with FDA. PDUFA meetings and advisory committee meetings with US FDA, EU scientific advisory committee. Regulations of Drugs and cosmetics Act, and its importance to Indian pharma industry. Recent regulatory changes in Indian DCGI and compiling dossiers for various DCGI submission: Hands on workshops in next 15 days: Word template of CTD structure. Hands on work of filling different regulatory forms in US/EU/India. Preparing for Regulatory interviews (Example interview questions will be provided). Communication skills. 2-3 seminars each of individual students to enhance their confidence and presentation skills. Explaining the real difficulties faced in a pharma industry and providing Corrective and Preventive Actions (CAPA). Training Duration (Classroom/Online): 3-Months/2-Months Training Fee: 20K/25k + Taxes Mobile: Website:- http://covalentech.com/regulatory_affairs.html

COVALENT:- Covalent is a group of company which has services and operations in Clinical, Information Technology, Energy, consumer products, Power and Infrastructure. Training @ Covalent:- We arededicated to establish ourselves as ''A values-driven organization''. These values will continue to direct our growth and organization’s operation. “Covalent” values supporting the way like “Kreative”. Training Duration (Classroom/Online): 3-Months/2-Months Training Fee: 20K/25k + Taxes Mobile: Website:- http://covalentech.com/regulatory_affairs.html

Groupware Training is offering Regulatory Affairs training in Hyderabad with real time faculties. To know more Contact: Mobile: +91-

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital.

Covalent is one of the leading training institutes for Regulatory Affairs in Hyderabad.Course Content of RA is Introduction to different types of Pharmaceutical products: Basic concepts on Rx, OTC, API, Starting material, DP/FP,Biologics vs. Biosimilars, Laws vs. Regulations vs. guidelines. Worldwide regulatory agencies and their role Approval process. Post-market regulatory obligations GLP’s: 21 CFR 58 -The History of GLP, The Idea behind GLP, The Areas of Application, The Pillars of Good Laboratory Practice,,Indian GLP and International GLP. CMC topics: GMP, Preformulation studies, ICH Q 7 guideline, 21 CFR 210 and 211, Medical device CE marking and ISO certifications.

RAAJ GLOBAL PHARMA REGULATORY AFFAIRS CONSULTANTS [RAAJ GPRAC], Thane-Mumbai is an ISO certified 29990-2010, and NSDC accredited institute for Pharma training and Upskilling.JOBS available with training into Global Regulatory Affairs, QA-QM, Clinical, PV, CTD/eCTD/ACTD/NeeS Regulatory submissions etc. 100% JOB Guarantee. Eligibility- B.Pharm, M.Pharm, B.Sc, M,Sc, B.Tech, M. Tech and Life sciences graduates and Pharma working professionals.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains studentswith hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM,SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room,Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research. Technical learning's: Extensive knowledge of drug safety and drug development process and procedures In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines Extensive knowledge of US and ICH safety reporting regulations and guidelines. Good understanding of IND safety reports, 21 CFR part 11 and HIPPA guidelines. Performed triage, evaluation and processing of adverse event reports from post marketing and clinical sources in accordance with FDA and ICH guidelines Working knowledge pertaining to MedDRA and WHO Drug dictionaries. Proficient in data entry and excellent knowledge of ARGUS safety database. Eligibility: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S/B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. MAIL ID: WEBSITE: www.igcp.co.in FOR ONLINE TIMINGS: PM TO PM FOR CLASS ROOM TIMINGS: AM TO PM ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE, # 2ND FLOOR,ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:,, 040 .

100% Job Oriented Medical Billing Coding/Medical Internship Training With Placements:- Organization at a Glance: Global Institute Of Advanced Pharmaceutical & Health Sciences (GIPHS) is a leading resource consulting services organization for the Pharmaceutical, Biotechnology and Medical Device industries. We Provide contract and permanent job opportunities within the Pharmaceutical, Biotechnology and Medical Device industries to experienced professionals as well as entry level candidates. The services offered fall into the broad categories of Recruitment Solutions, Temporary Staffing, Outsourcing, Consulting, Application Hands on Software Training in Clinical Data Management (Oracle Clinical, Oracle Inform/Central Designer), Pharmacovigilance (Oracle Argus Safety Database, Oracle AERS), CDISC SDTM, Medical Coding, Clinical Coding (MeDRA & WhoDrug Dictionaries) & SAS to aspirants of Clinical Research Industry. We successfully help the top Pharmaceutical, Biotechnology and Medical Device organizations from around the world to recruit high caliber experienced & trained professionals. Global Institute Of Advanced Pharmaceutical & Health Sciences (GIPHS) also provides Site Management Services, Clinical Data Management, Pharmacovigilance, Medical Writing, Medical Coding, Medical Billing, Biostatistical Analysis, SAS Programming & IT Support Services to Pharmaceutical, Biotechnology and Medical Device Organizations globally. Mode of Training- Classroom/Online Alternative day exams with focus on CPC and CCS Certification preparation. • Daily exams. • Physician and Hospital coding. GlPHS(Global Institute Of Advanced Pharmaceutical & Health Sciences)Labs Advantages: • Own Medical Coding live projects • Highest Placement record across all training institutes • Industry SOPs based training • Trainers with minimum 5 years experience The focus of the lectures will be mainly on the following topics: ICD Coding (Diagnosis Coding) CPT Coding (Procedures Coding) HCPCS Coding (Supplies Coding/Drugs Coding), Hospital Coding CPC and CCS Preparation HIPAA ComplianceICD Coding (Diagnosis Coding) CPT Coding (Procedures Coding) HCPCS Coding (Supplies Coding/Drugs Coding) Hospital Coding • CPC and CCS Preparation • HIPAA Compliance Clinical Coding • MedDRA • Structure and Content • Comparison to COSTART • Coding and the Points to Consider Document • Standardized MedDRA Queries (SMQs) • Versioning • CTCAE Mapping to MedDRA • Regulatory Expectations • Overview of the MedDRA dictionary (structure and format) • General coding principals based on the current MedDRA Points to Consider • Practical exercises in MedDRA coding • General analysis and reporting principals based on the current MedDRA Data Retrieval and Presentation: Points to Consider • Practical exercises in MedDRA analysis and reporting • Review of MedDRA • Rules and Conventions Used In MedDRA • MedDRA Term Selection: Points to Consider Document • Discussion of the Coding Examples Provided in the “Points to Consider” Document • Additional Coding Examples to Further Explain the Term Selection Points • Importance of Company Coding Conventions • WHO Drug • Review of WHO Drug • Identifying the Drug • Using a "Fuzzy" Search Engine • Search Using Google • Martindale Online • Other Web Resources • General Principles for Selecting the Appropriate WHO Drug Entry • Abbreviations • Handling Drugs with Multiple WHO Drug Entries • Special Rules for Coding Certain Drugs and Drug Categories • Multi-Ingredient Drugs • Querying Terms • Importance of Company Coding Conventions • Change Request Process • Coding Herbal Medicines • Coding Investigational Products • Coding Vaccines • Coding Multivitamins • Handling Reported Non-Therapies • Application and Use of ATC Codes • Practical Exercises in WHO Drug Coding • The Following Chapters are discussed in detail • Integumentary System coding • Musculoskeletal System coding • Respiratory System coding • Cardiovascular System coding • Digestive System coding • GenitoUrinary System coding • Neurology coding • Sense Organs coding • Radiology coding • Pathology coding • Medicine coding and Medical Billing in detail • HIPAA compliance • This course will provide training in the core competencies in Medical Coding including fundamentals of clinical trials. It's a great program for industry professionals who are looking to advance their careers or seeking industry certifications and anyone looking to enter the clinical research & Health Care Industry. We are certified members of American Academy of Professional Coders. GIPHS (Global Institute Of Advanced Pharmaceutical & Health Sciences Comprehensive Medical Coding training program provides you with the training and practical experience you need to develop the skills necessary to work as a medical coding and billing professional. Prepares you to perfection to pass national medical coding certification exams Covers the complete syllabus and meets requirements for both the AHIMA and AAPC certification exams, including the CCA, CPC, and CPC-H. As a certified coder, you will be in high demand in the job market. Instructors with Onsite/Real time experience and Certified in the field. Instructors have "been there, done that" and know not only what it takes to create career opportunities in your field of interest but also how you'll be able to apply your industry-current education once you make your move. Career-focused training programs with concentrations to help you build relevant credentials Live Project Training with Internship will also be provided in Health Care BPOs. Mode of training- Instructor Led Class room/ Online Training Tenure: 2 month Eligibility Applicants are recommended to have Any life Science degrees: Bachelor's(B.Sc Life Sciences), Master’s (M.Sc Life Sciences), or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (companies, CROs and Hospitals. Certification: Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by Global Institute Of Advanced Pharmaceutical & Health Sciences For more information, please contact Global Institute of Advanced Pharmaceutical & Health Sciences at Training Location (Venue) GIPHS (Global Institute of Advanced Pharmaceutical & Health Sciences) Academy of Clinical Research KVR Enclave, #nd Floor,Beside Satyam Theater,Near Maitrivanam, Ameerpet, Hyderabad. Contact Information Dr.Anita Singh Training Coordinator Mob No:+91

SAP Global Trade Services online training SAP Global Trade Services Overview (GTS) SAP Global Trade Services (SAP GTS) automates global trade processes and enables you to manage large numbers of business partners and high volumes of documents, while also helping you to comply with changing legal regulations. It facilitates global trade by providing you with the tools you require to respond to governments modernizing their systems and to customs authorities communicating electronically with businesses. SAP Global Trade Services (SAP GTS),can manage all the complexities of international trade including full regulatory compliance, electronic communication with customs authorities, and risk mitigation, while importing and exporting on a global basis. Business Content for SAP GTS enables you to analyze your import and export transactions and perform strategic reporting for the following areas: SAP Customs Management: "Customs Processing" service SAP Customs Management: "Transit Procedure" service SAP Risk Management: "Preference Processing" service SAP Risk Management: "Restitution" service SAP Compliance Management: "Import/Export Legal Control" service A large amount of transaction data and master data is available in SAP GTS. A selection of the data is extracted into SAP NetWeaver Business Intelligence (BI) and evaluated there. Online Training Features 1. Interactive Learning sessions 2. Industry Savvy Trainers 3. Learn Right from Your Place 4. Customized Curriculum 5. Highly Affordable Courses 6. Support after Training 7. Placement Services for H1B / EAD status holders* About Acutesoft ACUTE SOFT is a Global Interactive Learning company started by proven industry experts with an aim to provide Quality Training in the latest IT Technologies. ACUTE SOFT has a pool of Expert Trainers worldwide on all the technologies to train the students. ACUTE SOFT is offering online Training services to Major IT giants and to individual students worldwide. We also provide online training on SAP FICO,SAP SD,SAP WM,SAP PP,SAP MM,SAP SRM,SAP FSCM,SAP MDM,SAP APO, SAP IS RETAIL,SAP CRM,SAP ABAP,SAP BI,SAP BASIS,SAP BO,SAP HANA,SAP BPC,SAP ESS-MSS,SAP CS,SAP PLM,SAP GTS And SAP SNC. Experience the Quality of our Online Training. For Free Demo Please Contact Santhosh /Lakshmi: INDIA: +91-9848346149, +91-7702226149 Land line: +91 (0)40 - 42627705 US: +1 973-619-0109, +1 312-235-6527 UK :+44 207-993-2319 Skype id : acutesoft http://www.acutesoft.com http://training.acutesoft.com

Overview: SAP GRC Access Control is a suite of capabilities that monitor, test, and enforce access and authorization controls across the enterprise. SAP GRC Access Control helps companies to comply with regulatory mandates such as Sarbanes-Oxley. Organizations can readily identify and remove access and authorization risks from IT systems, as well as embed preventive controls in business processes to stop segregation of duties (SoD) violations. Hi, Greetings of the day. ABOUT ECORPTRAININGS: Ecorp Trainings are one of the best institute providing quality level of training in E-learning process.This is instructor led online training. We also provide corporate training , if group of people interested in same technology. Contact us for detailed course content & register for a free demo. We also provide support in client interviews , resume preparation , ticket resolving. Contact us for custom designed training course by experts exclusively for yourself. We provide training for almost all IT technologies i.e ; JAVA , DOTNET , SAP ,ORACLE , PEOPLESOFT ,HYPERION etc, contact us if you have any particular need. ECORP TRAININGS. Gtalk ID : ecorptrainings Skype ID : ecorptrainings

Overview: OpenText software applications manage content or unstructured data for most types of governance, efficiency and monetization requirements in large companies, government agencies and professional service firms. OpenText solutions are aimed at addressing information management requirements, including the management of large volumes of content compliance with regulatory requirements, and mobile and online experience management. ABOUT ECORPTRAININGS: Ecorp Trainings are one of the best institute providing quality level of training in E-learning process.This is instructor led online training. We also provide corporate training , if group of people interested in same technology. Contact us for detailed course content & register for a free demo. We also provide support in client interviews , resume preparation , ticket resolving. Contact us for custom designed training course by experts exclusively for yourself. We provide training for almost all IT technologies i.e ; JAVA , DOTNET , SAP ,ORACLE , PEOPLESOFT ,HYPERION etc, contact us if you have any particular need. ECORP TRAININGS. Gtalk ID : ecorptrainings Skype ID : ecorptrainings

Overview: TrackWise SelectStart is a purpose-built quality management solution created specifically for emerging pharmaceutical and biotechnology companies. Organizations in this phase of growth are faced with the same rigorous quality and regulatory requirements as multibillion-dollar organizations, while not having the same expansive resources and budget. ABOUT ECORPTRAININGS: Ecorp Trainings are one of the best institute providing quality level of training in E-learning process.This is instructor led online training. We also provide corporate training , if group of people interested in same technology. Contact us for detailed course content & register for a free demo. We also provide support in client interviews , resume preparation , ticket resolving. Contact us for custom designed training course by experts exclusively for yourself. We provide training for almost all IT technologies i.e ; JAVA , DOTNET , SAP ,ORACLE , PEOPLESOFT ,HYPERION etc, contact us if you have any particular need. ECORP TRAININGS. Gtalk ID : ecorptrainings Skype ID : ecorptrainings

Pharmacovigilance Training & Placements The course modules cover theoretical aspects of pharmacovigilance through a structured curriculum. The course will put emphasis on interactive sessions with the participants, hands-on approach on the Argus database with case assignments, group discussions and quizzes as evaluation components Overview of Pharmacovigilance Regulatory Aspects of Pharmacovigilance Periodic Safety Updates Reports(PSUR's) Suspected Unsuspected Serious Adverse Reactions Care Reporting Process Eudra Vigilance Signal detection Process and tools Safety Intelligence Practical and Hands- on Oracle Argus Data Base Eligibility criteria for admission Applicant should have a Bachelor’s or Master’s Pharmacy & MBBS And All Medicine Students. Pharmacovigilance is a growing sector. With increased outsourcing and the advent of tightened regulations by the regulators, there will be a lot of scope for professionals who are ‘pharmacovigilance-ready’. The placement opportunities can be from CROs, BPOs or Pharmaceutical companies. Course Duaration: 2months (50) Contact: Lara Clinical Research #nd floor,Nilgiri Block,Aditya Enclave Ameerpet,Hyderabad Get Trained and Placed in Pharma, CRO, MNC Industries Do you have a Background in Science, Medicine or Related Area? Do you wish to pursue a career in Clinical Research Industry? Do you wish to become a Clinical Research professional? Do you wish to become a Clinical Data Professional? Do you wish to become a SAS Programmer or Analyst? Do you wish to become a Drug safety Associate (PV) Professional? Do you wish to become a Medical Coder professional? If your answer to any of the above question is “YES” then Contact us to get you started on diverse Training opportunities in Lara Clinical Research Training Institute. Lara Clinical assists life science and healthcare professionals achieve success by delivering specific solutions for their individual needs, our Popular Training Programmes. Course Curriculum: 1)Clinical Research & Data Management 2)Clinical Data Management & Pharmacovigilance 3)Clinical Data Management with SAS Clinical Programming 4)Pharmaco vigilance 5)Medical Coding 6)CDISC/SDTM 7)SAS-Clinical To enroll in any of these courses and packages tailored to to your needs contact at any by emailing Lara Clinical Research, Ameerpet Hyderabad Calling Pharmacy professionals, Medicine professionals, Life science Studnets, IT Students Training will be conducted in Hyderabad Ph: 040-,

SAP QM – Quality Management SAP QMIntroduction Description: SAP Quality Management (QM) assures that products meet stringent regulatory standards, are safe and uniform, and meet company product specifications. SAP QM processes are thoroughly integrated into the manufacturing process. What you Learn Course Goals: Business Process HowQM Module work in R/3 Implementation Training Integration with other Modules Real-time Training with End to End Implementation Process.

Have you always wanted to be a ship captain? Does the sound of crashing waves against a ship’s bow give you a charge? If so, maybe it’s time to start your nautical career with deck officer training at the International Maritime Academy. With a quality education in maritime sciences your international employment opportunities are limitless. As a Deck Officer you will be the authoritative person on board maritime and merchant ships. From sorting out regulatory issues to quality control to clash determination and dispute resolution you will be a leader. Not ready for a leadership role? As a Chief Mate you support the Deck Officer, ensuring smooth ship operation on a day-to-day basis. At the International Maritime Academy you will gain practical, hands on, sea experience during your Merchant Navy Course Training. Don’t wait! Begin your nautical career by visiting us

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management,CDISC-SDTM, and SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains students with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance,Drug regulatory affairs, Table Listings Figures (TLF’S)etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research.

Institute of Good Clinical Practice (iGCP) offers different unique programs for aspiring professionals willing to pursue a career in Clinical Research, Clinical Data Management, CDISC-SDTM, SAS. The training program aims to provide a career path for professionals from Life Sciences and Statistics background. Highly experienced staffs from clinical research and data management industry trains you with hands on experience on various areas in clinical research, Clinical Data Management, CDISC-SDTM, SAS, Pharmacovigilance, Drug regulatory affairs,etc. Institute of Good Clinical Practice (iGCP) provide training in three different modes like Class Room, Online-learning for all Medical, Pharmacy and Science students and professionals aspiring to make a career in Clinical Research.

Clinnovo Research Labs is a biopharmaceutical services company, provides a range of clinical research, consulting, and technology products and services to the pharmaceutical, biotechnology, and medical device industries worldwide. Clinnovo group of companies was founded in 2005 and is headquartered in Hyderabad, India. Clinnovo Offers Services & Training In Clinical Research Course, Clinical Data Management Training, Sas, SDTM, ADaM, Medical Coding, Imaging, Pharmacovigilance and Drug Regulatory Affairs. Online Clinical Course, Class Room, Pg Diploma, Internships Available.

Clinnovo Offers Services & Training In Clinical Research Course, Clinical Data Management Training, Sas, SDTM, ADaM, Medical Coding, Imaging, Pharmacovigilance and Drug Regulatory Affairs. Online Clinical Course, Class Room, Pg Diploma, Internships Available

To be a doctor in the UK, one need to have good communication skills and should be able to speak English fluently. OET exam score comes in grade like A, B, C, D and E. BAFEL, speciality in English helps doctors to pass OET examination with grade B in all areas. A minimum of B grade in each of the 4 subject is required to clear the exam and it is valid upto 2 years. We provide best OET training for doctors which helps a candidate to achieve desired results. All our trainers are OET teachers are capable of giving best training in their respective fields. The OET test for doctors is recognised by a wide range of regulatory healthcare bodies and councils in the UK, Ireland, New Zealand and various other countries. BAFEL provides interactive and practical approach to OET led by our teams of highly experienced OET teacher. Call now for more enquiries on OET for doctors at BAFEL.

Pharmacovigilance online training Pharmacovigilance Basic: Legal basis for safety coverage as well as a historical perspective Basic definitions and tools Pre- and Post-marketing: Basic variations Pre-Marketed AEs Post-Marketed AEs The Importance of Adverse Event coverage Suspected sudden Serious Adverse Reaction Sources of ADRs Causality Lack of effectiveness Expectedness Minimum Criteria for coverage Expedited coverage An introduction to the Eudravigilance system Qualified Person for Pharmacovigilance (QPPV) needs Development Safety Update Reports European communication laws New EU Pharmacovigilance Legislation Pharmacovigilance Advanced: Types of Audits & Inspections Approaches Preparing for a Pharmacovigilance scrutiny Overview of the Pharmacovigilance Audit Best Practices Detailed Audit things Need for detection The Cost of Failure Signalling summary Regulatory needs Signal Detection Objectives Incidence, Numerator, divisor Need for the ready Mind Signal Detection Hierarchy Approach to detection Signalling Examples Risk assessment and management For more details: Hno , road no: 3 New Dilshuknagar nagar colony Dilshuknagar,Hyderabad – ,India Mobi No:+, Land line No: 040

ARETE Company is providing Pharmacovigilance training,free placements, & internship certification.This course includes Clinical Data Management,Clinical research,Regulatory Affairs,Reporting systems.Duration of this course is 2 months interested ones can contact us through the given details hurry up offer will end soon. #arete #Pharmacovigilance #medicalcoding #clinicalsas # vijayawada #Visakhapatnam #Hyderabad #tirupati

Oracle Identity Management -8179736190 We are providing Oracle Identity Management (OIM) under Yashwanth, MTech, and Technical Manager in CMMI Level 5 Company with 9+ years of middleware experience Oracle Identity Management is a complete and integrated, next-generation identity management platform that provides breakthrough scalability; enables organizations to achieve rapid compliance with regulatory mandates; secures sensitive applications and data regardless of whether they are hosted on-premise or in a cloud; and reduces operational costs. Course Contents • Introduction • Identity Management: Overview • Understanding Oracle Identity Manager • Installing and Configuring Oracle Database • Installing and Configuring Oracle Weblogic Server • Installing and Configuring Schema for OID & OVD using RCU • Installing and Configuring Identity Management Suite • Upgrading Database Schema for Identity Management • Installing and Configuring Oracle Identity Manager • Starting and Understanding Oracle Identity Manager Consoles • Managing Users and User Entities • Using Predefined Connectors • Assigning Oracle Identity Manager Connectors to Users • Provisioning User Resources Manually • Provisioning User Resources Automatically • Expanding the Provisioning Workflow • Approving the Provisioning Workflow • Understanding Reconciliation • Performing Reconciliation • Understanding and Using Attestation Processes • Customizing the OIM Administrative and User Console

Oracle Identity Management -8179736190 We are providing Oracle Identity Management (OIM) under Yashwanth, MTech, and Technical Manager in CMMI Level 5 Company with 9+ years of middleware experience Oracle Identity Management is a complete and integrated, next-generation identity management platform that provides breakthrough scalability; enables organizations to achieve rapid compliance with regulatory mandates; secures sensitive applications and data regardless of whether they are hosted on-premise or in a cloud; and reduces operational costs. Course Contents • Introduction • Identity Management: Overview • Understanding Oracle Identity Manager • Installing and Configuring Oracle Database • Installing and Configuring Oracle Weblogic Server • Installing and Configuring Schema for OID & OVD using RCU • Installing and Configuring Identity Management Suite • Upgrading Database Schema for Identity Management • Installing and Configuring Oracle Identity Manager • Starting and Understanding Oracle Identity Manager Consoles • Managing Users and User Entities • Using Predefined Connectors • Assigning Oracle Identity Manager Connectors to Users • Provisioning User Resources Manually • Provisioning User Resources Automatically • Expanding the Provisioning Workflow • Approving the Provisioning Workflow • Understanding Reconciliation • Performing Reconciliation • Understanding and Using Attestation Processes • Customizing the OIM Administrative and User Console

Learn important & required concepts related to clinical sas programming which is a blend of base sas, advance sas & CDISC SDTM standards. Describe the clinical research process (phases, key roles, and key organizations). Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices). Read more:

GUIDANCE AVAILABLE FOR BASIC TO ADVANCE ONLINE SHARE TRADING CLASSES COURSE CONTENTS: 1] BASIC INTRADAY/ DAY TRADING COURSE DURATION: TOTAL HRS [plus one month on-line support through chat during market hours once you open your demat account with us. With this I will monitor your trading on day to day basis plus we will guide you through live market to teach you how to first remain safe at all the time and at the end of day make appropriate profit in any market situation. In this you will start receiving Live market calls [Delivery/ Intraday/F&O] to start learning the online trading techniques and earning slowly but consistently to become a successful trader or an Investor in due course of time. FEES – RS./- PLUS TAXES AT ACTUAL IF PAYMENT MADE BY CHEQUE. 1] Introduction to capital markets, 2] Pre market reports, BSE/NSE conceptual along with Sensex and Nifty concept. 3] And how they work hand in hand with different profit centers, 4] Discussion on important sectors, 5] Basic study for Sensex and Nifty for Intraday / Day trading, 6] Important acts one must do as beginner during trading, 7] Stop loss concept, 8] Pay-in / pay-out concepts, 9] Difference between day trading and delivery trading, 10] Day trading key notes / indicators one needs to follow all the time during trading hours, 11] Intraday / day trading key formula’s- Total 6Nos, 12] Circuits- conceptual and their importance during trading, 2] ADVANCE- DERIVATIVES [GUIDE TO FUTURE’S & OPTION’S] COURSE DURATION: TOTAL HRS [Plus one month on-line support through chat during market hours once you open your demat account. In that you will start receiving Live market calls [Delivery/Intraday/F&O] FREE to start learning the online trading techniques and earning slowly but consistently to become a successful trader or an Investor. FEES – RS./- PLUS TAXES AT ACTUAL IF PAYMENT MADE BY CHEQUE. 1] Introduction to securities market, 2] Introduction to derivatives Market, 3] Introduction to futures, 4] Pricing of futures, 5] Using index futures, using stock futures, 6] Introduction to options, Pricing of options, 7] Using Index Options, Using of stock options, 8] Open interest, Margins- Clearing & settlement in F&O, 9] Corporate Adjustments, Regulatory Framework, 10] Future & option Contract specification, 11] How to enter Future & option market, 12] How to trade In Future & option market, 13] Factors influencing the market, Sources of information, Taxation etc. IF YOU OPT FOR BOTH THE MODULES [BASIC + ADVANCE] AT ONE SHOT YOU HAVE TO JUST PAY RS./- PLUS TAXES AS APPLICABLE IF YOU PAY BY CHEQUE. CLASSES AT YOUR DOOR STEP WILL BE CONDUCTED ON ALL WEEK DAYS WITH MUTUALLY DECIDED DAY AND TIME EXCEPT MARKET HOURS FROM MONDAY TO FRIDAY. SPECIAL WEEK END SESSIONS OR MORE CLASS HOURS IS VERY MUCH POSSIBLE ON ALL WEEK DAYS POST MARKET HOURS BETWEEN 4.30PM TO 8.30PM

In today’s regulatory environment to store large amount of data and structure of data is being hard. But by using Mongo DB we can do that. Are you looking for a Mongo DB then you have to join Suntrainings in Hyderabad. Our institute provides online, classroom, corporate batches to the students. we provide job assistance for the eligible student.our trainers are having 10+ years of experience with real time projects.our contact details are: Phone: +91 9642434362

In today’s regulatory environment to store large amount of data and structure of data is being hard. But by using Mongo DB we can do that. Are you looking for a Mongo DB then you have to join RS Trainings in Hyderabad. Our institute provides online, classroom, corporate batches to the students. we provide job assistance for the eligible student.our trainers are having 10+ years of experience with real time projects.our contact details are: Phone: +91-905-269-9906 COURSE CONTENT: • Installation and Administration • Installing Mongo DB • Starting and stopping Mongo DB servers • The JavaScript console Mongo DB Basics • Servers • Databases • Collections Documents / Objects • CRUD • Indexes • Clients and drivers • Overview and integration Building applications with Mongo DB • Overview • Getting started • Examples and labs • Advanced querying • Projections • Conditional operators • Limit and skip • Aggregation and grouping • Performance and scaling • Master / slave • Sharding

Introduction to different types of Pharmaceutical products: Basic concepts on Rx, OTC, API, Starting material, DP/FP, Generics vs. Innovator drugs, Biologics vs. Biosimilars, Laws vs. Regulations vs. guidelines. Drug discovery and development Worldwide regulatory agencies and their role