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Argus safety configuration


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Hyderabad (Andhra Pradesh)
Type Training Institute GIPHS Is Providing Pharmacovigilance Training on Oracle Argus Safety Database 7.0. With MedDRA & WHODD Medical Coding.GIPHS (Global Institute OF Advanced Pharmaceutical & Health Sciences) is a leading resource consulting services organization for the Pharmaceutical, Biotechnology and Medical Device industries. We offer contract and permanent job opportunities within the Pharmaceutical, Biotechnology and Medical Device industries to both experienced professionals and entry level candidates. The services offered fall into the broad categories of Recruitment Solutions, Temporary Staffing, Outsourcing, Consulting, Application Training in Clinical Data Management (Oracle Clinical, Oracle Inform/Central Designer), Pharmacovigilance (Oracle Argus Safety Database, Oracle AERS), CDISC SDTM & SAS to aspirants of Clinical Research Industry. We successfully help some of the top Pharmaceutical, Biotechnology and Medical Device organizations from around the world to recruit high caliber experienced & trained professionals.
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India
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.
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India
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 .
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India
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. 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 .
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India
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 .
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Hyderabad (Andhra Pradesh)
Type Training Institute GIPHS Providing Pharmacovigilance Training On Oracle Argus Safety Database 7.0.3 Version With MedDAR and WHODD Medical Coding.
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Hyderabad (Andhra Pradesh)
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
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Hyderabad (Andhra Pradesh)
Type Training Institute GIPHS Providing Pharmacovigilance Training On Oracle Argus Safety Databasse 7.0 With MedDRA and WHODD Medical Coding
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India (All cities)
ADVANCED CERTIFIED PHARMACOVIGILANCE TRAINING WITH HANDS ON TRAINING IN ORACLE ARGUS SAFETY DATABASE, MedDRA & WHODD Browsers with 100 % placements Assistance. Organization at a Glance: Gratisol Labs is a leading resource consulting services organization for the Pharmaceutical, Biotechnology and Medical Device industries. We offer contract and permanent job opportunities within the Pharmaceutical, Biotechnology and Medical Device industries to both experienced professionals andss entry level...
₹ 8.000.000.000
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India
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-,
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Hyderabad (Andhra Pradesh)
SAP EHS Online Training all over the world KBS Training Institute is providing exclusive training on SAP EHS (+91 - India) Online Training in Hyderabad, Bangalore, Mumbai, Chennai, Pune, Singapore, Malaysia USA, Canada, UK, France, Japan, Germany, Dubai, Newzeland, Australia, Middle East, GCC, UAE (Dubai, Abu Dhabi), Saudi Arabia, Qatar, Bahrain, Oman, Kuwait and etc. Our Training Importance % job assurance 2. Quality based education. 3. Providing global exposure for the students 4. Real time experience over training 5. Getting experience over a full life cycle project Implementations Course Overview SAP EHS supports the management of industrial hygiene, safety, and occupational health processes. SAP EHS Management helps you ensure compliance with regulations for product safety, hazardous substances, dangerous goods, and waste management. SAP Product Lifecycle Management (SAP PLM) addresses a range of environment, health, and safety issues. Course Content • SAP EHS Product Safety Training • SAP EHS WWI Template Training • SAP EHS Expert Training • SAP EHS Configuration Training • Languages, native language support • Integration between EHS, Material Master, and Sales and Distribution; output determination; Document Management System • Classification system • Units of measure • Conclusion KBS Training Institute provide all course material and the real time experts teaches the trainees at any time which are flexible timings to the students, After training also we will support the qualified students like mock interviews, CV preparation and etc. Contact Details: KBS Training Institute, K.V.Rao, +91 , India - Hyderabad - Bangalore.
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Bangalore (Karnataka)
Type Computer Softgen Infotech located in BTM Layout, Bangalore is a leading training institute providing real-time and placement oriented SQL Server Training Courses in bangalore. Our SQL Server training course includes basic to advanced levels. we have a team of certified trainers who are working professionals with hands on real time SQL Server projects knowledge which will provide you an edge over other training institutes. Our SQL Server training centre is well equipped with lab facilities and excellent infrastructure for providing you real time training experience. We also provide certification training programs in SQL Server Training. We have successfully trained and provided placement for many of our students in major MNC Companies, after successful completion of the course. We provide placement support for our students. Our team of experts at Softgen Infotech Training Institute, Bangalore have designed our SQL Server Training course content and syllabus based on students requirements to achieve everyone's career goal. Our SQL Server Training course fee is economical and tailor-made based on training requirement. We Provide regular training classes(day time classes), weekend training classes, and fast track training classes for SQL Server Training in our centres located across bangalore. We also provide Online Training Classes for SQL Server Training Course. Contact us today to schedule a free demo and complete course details on SQL Server Training Course. What is SQL Server Training ? SQL Server Training Objectives Installing Microsoft SQL ServerUpgrading to SQL Server Management StudioMonitoring the Database ServerDatabase and Index MaintenanceUsing the Database Tuning AdvisorSQL Server Disaster RecoveryDatabase AvailabilityReplicating InformationHTTP Synchronization for Merge ReplicationOLE DB Command objectMonitoring and Performance Training Prerequesites Any Programming Language Knowledge.Good understanding of relational databasesSome experience with client databases, such as Access. Course Details SQL Server Overview Availability and Scalability Features Security Features Data Management Features Administration and Maintenance Features Development Features To enable SQLiMail Testing mail delivery Installing SQL Server SQL Server Editions Installing Microsoft SQL Server System Requirements Preparing for a SQL Installation Installation Checklist Setup Features Using the System Consistency Checker Component Install Unattended Installation Installation Sequence Installation Maintenance Upgrading to SQL Server Management Studio Management Studio Windows Registered Servers Object Explorer Review Database Objects Modify Database Properties Create Database Scripts The Maintenance Plans Node Solution Explorer Query Editor Template Explorer Dynamic Help Upgrading to SQL Server Computer Manager SQL Server Services node SQL Server Network Configuration node SQL Server Native Client Configuration node The SQLCMD Management Utility SQLCMD Syntax SQLCMD Variables Dedicated Administrative Connection SQL Server Management Studio SQLCMD Mode Securing SQL Server Implementing Securable New Security Features Principals Securable Permissions Permission Types Managing Logins Managing Schemas Managing Users Schema Definition Using Schemas Managing Execution Context Managing Permissions Manage Server Permissions Manage Server-Scope Securable Permissions Manage Database Permissions Manage Database-Scope Securable Permissions Native Data Encryption Code and Module Signing Database Availability SQL Data Availability Database Mirroring The Witness Server and Automatic Failover Configuring Database Mirroring Transaction Safety Level Operating Modes High Availability Operating Mode High Protection Operating Mode High Performance Operating Mode Monitoring Mirroring Database States for Database Mirroring Prepare the Servers Configure Mirroring Verify Principal and Mirror Access Execute the Mirror Failover Verify Mirror and Witness Status Terminating the Mirror Session SQL Server Integration Services Creating the Database Objects Creating a Package Using Business Intelligence Studio Integration Services Project Template OLE DB Command object Column Mappings Adding a Data Viewer Monitoring the Database Server Managing Metadata Views Metadata Storage System Views Information Schema Catalog Views Sys All Dynamic Management Views System Stored Procedures Database and Index Maintenance Index Management New Index Features Creating Indexes Online Index Maintenance Parallel (multiple CPU) Index Operations Lock Options Included Columns in Indexes Partitioned Tables and Indexes XML Index Support Altering an Index Rebuilding an Index Reorganizing an Index Disabling an Index Dropping an Index Index Fragmentation Using the Database Tuning Advisor SQL Server Disaster Recovery Disaster Recovery SQL Disaster Recovery Feature Enhanced Features Database Snapshots Creating a Snapshot Common Snapshot Applications Undeleting table rows Undoing a table update Recovering a dropped object Backup and Restore Media Integrity Changes Recovering the MASTER Database Create a mirrored backup Restore from the backup mirror Create a snapshot Restore the snapshot data Automate the creation of daily snapshots Replicating Information Replication Enhancements Stand-alone Replication Monitor Support for Oracle Publishing HTTP Synchronization for Merge Replication Subscriber Initialization Replicating DDL Statements Modified User Interface Replication Management Objects To Configure Publishing and Distribution Configuring Peer-to-Peer Replication Create a Publication Create a Subscription with RMO Monitoring and Performance SQL Server Profiler Optimal Data Storage Diagnostic Tools Query Analyzer Database Engine Tuning Advisor Index Optimization Federated Database Servers Partitioned Indexes Lock Optimization SQL Server Training Course Details Duration:30 Hours Version:latest Version Regular: 1 Hour per day Fast Track: 2 - 3 Hours per day: 10 days Weekdays:Monday - Friday Weekend:Saturday and Sunday Online Training:Available Class Room Training: Available Course Fee: Talk to our Customer Support Mode of Payment:Talk to our Customer Support
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India
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Mumbai (Maharashtra)
The Database Administrator is responsible for managing, observing, and maintaining the Oracle database infrastructure. The Oracle DB will also make use of and improve the definite policies and procedures for making sure the safety and reliability of the Oracle environment. The DB tasks will include creating and sustaining Oracle databases, actively offers performance observation and solve performance issues, offer Oracle resource capacity management solutions, configuration, execution, and supervising of database backups. In addition to this, the DBA will supply technical proficiency to the development organization. VirtualNuggets offering the perfect training solutions for our participants. We at Virtualnuggets are providing Oracle DBA online training supported by the latest cutting-edge learning techniques and tools, our online training experts provide excellent training to help our Global wide online participants to thrive with Oracle DBA career and to excel their professional life. For more in information on Oracle DBA mail us to info(at)virtualnuggets(dot)com, and visit our website
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