Placement cr pharmacovigilance cdm

Gratisol Labs is a leading contract research organization (CRO) and with our "Academy of Clinical Research" we offer an extensive but economical and short duration Employment Oriented Certification Programs in Clinical Research and Pharmacovigilance which will help you achieve a bright career in the mentioned domains. Gratisol Labs "Academy of Clinical Research"- THE INSTITUTE HAVING THE BEST PLACEMENT RECORD IN INDIA. Growth and Demand in Clinical Research Industry:- It is certain that in future as the number of clinical projects expands, there will be demand for qualified personnel in Clinical Research and Pharmacovigilance. The global clinical trial outsourcing opportunity in India in the pharmaceutical industry is estimated to be around $4 billion by and there will be requirement of clinical research professionals with lucrative salary range. Trained pharmacists and clinicians can plug this wide gap. They will be involved in the various aspects of clinical research starting from site-monitoring, site-management, clinical data management, data analysis, report writing, report submission, presentation and publication. Our Training Objectives: To provide extensive knowledge and understanding to the student to help him/her crack any interview at any global or Indian pharmaceutical company/ CRO. Certification: Successful candidates would receive a Certificate of Completion from Gratisol Labs. Emphasis: Special focus on interview skills via practice interview sessions. Our Training/Ceritification Program:- From 02nd May Gratisol is going to start its Regular Batch on Placement Program in Clinical Research, Clinical Data Management and Pharmacovigilance Features of the program:- 1. Start Date:- 02nd May, . Duration:- 2 Months 3. Classes will be held on Monday, Tuesday, Thursday and Friday. 4. Class Duration:- 1.5 Hours/Day 5. Fee:- Rs. /-(Rs. /- for anyone paying it at start as one time payment) 6. Maximum Seat:- 8 Students Only * Please note that from the month of May, Certification Program Fees for both Regular and Weekend Program will be Rs. /-(Rs. /- for anyone paying it at start as one time payment). PLACEMENT SUPPORT Extensive placement support would be provided to the successful candidates. Resume Development -- Guidance on ways to develop impressive and professional resume.That is why our success rate in terms of Placement is best in the industry, and we are striving hard to make it better. May be you will not be confident that you get placed or not, but we are sure enough that we will make a way through for you to get success.

Gratisol Labs is a leading contract research organization (CRO) and with our "Academy of Clinical Research" we offer an extensive but economical and short duration Employment Oriented Certification Programs in Clinical Research and Pharmacovigilance which will help you achieve a bright career in the mentioned domains. Gratisol Labs "Academy of Clinical Research"- THE INSTITUTE HAVING THE BEST PLACEMENT RECORD IN INDIA. Our Training/Ceritification Program:- From 02nd May Gratisol is going to start its Regular Batch on Placement Program in Clinical Research, Clinical Data Management and Pharmacovigilance Features of the program:- 1. Start Date:- 02nd May, . Duration:- 2 Months 3. Classes will be held on Monday, Tuesday, Thursday and Friday. 4. Class Duration:- 1.5 Hours/Day 5. Fee:- Rs. /-(Rs. /- for anyone paying it at start as one time payment) 6. Maximum Seat:- 8 Students Only * Please note that from the month of May, Certification Program Fees for both Regular and Weekend Program will be Rs. /-(Rs. /- for anyone paying it at start as one time payment). PLACEMENT SUPPORT Extensive placement support would be provided to the successful candidates. Resume Development -- Guidance on ways to develop impressive and professional resume.That is why our success rate in terms of Placement is best in the industry, and we are striving hard to make it better. May be you will not be confident that you get placed or not, but we are sure enough that we will make a way through for you to get success.

Gratisol Labs is a leading contract research organization (CRO) and with our "Academy of Clinical Research" we offer an extensive but economical and short duration Employment Oriented Certification Programs in Clinical Research and Pharmacovigilance which will help you achieve a bright career in the mentioned domains. Gratisol Labs "Academy of Clinical Research"- THE INSTITUTE HAVING THE BEST PLACEMENT RECORD IN INDIA. Our Training/Ceritification Program:- From 10th May Gratisol is going to start its Regular Batch on Placement Program in Clinical Research, Clinical Data Management and Pharmacovigilance Features of the program:- 1. Start Date:- 10th May, . Duration:- 2 Months 3. Classes will be held on Monday, Tuesday, Thursday and Friday. 4. Class Duration:- 1.5 Hours/Day 5. Fee:- Rs. /-(Rs. /- for anyone paying it at start as one time payment) 6. Maximum Seat:- 8 Students Only * Please note that from the month of May, Certification Program Fees for both Regular and Weekend Program will be Rs. /-(Rs. /- for anyone paying it at start as one time payment). PLACEMENT SUPPORT Extensive placement support would be provided to the successful candidates. Resume Development -- Guidance on ways to develop impressive and professional resume.That is why our success rate in terms of Placement is best in the industry, and we are striving hard to make it better. May be you will not be confident that you get placed or not, but we are sure enough that we will make a way through for you to get success. Email: Mobile number:

VRX Technologies is a premier Software and web solutions company,Provide Training and Placement Services. Pharmacovigilance Training. Training Period- Duration- 30 Days Duration-60 Days Duration-90 Days Online Class Room Training and Corporate Within this Training We will Provide Below Services- 5 Guaranteed MNC Interviews Provide High quality and Cost effective Training Certificate will be issued after Training Guest Lecture will be given During the courses. If you are interested then - Visit our below Office address. Address -Vrx Technologies,(A Software Training Institute) Near to Patny Bus Stop, Sec Paradise, Opposit to Taj Trister Hotel, CMR Building,3rd floor 302. Timing- 9.30 am to 6 pm.

OUR OBJECTIVE: TO IMPART PRACTICAL TRAINING ON CLINICAL RESEARCH / DATA MANAGEMENT AS PER ICH GCP GUIDELINES, LOCAL REGULATORY GUIDELINES AND ETHICAL GUIDELINES AND PROVIDE ‘INDUSTRY READY RESOURCES’ TO THE CLINICAL RESEARCH INDUSTRY AND THEREBY CONTRIBUTE TOWARDS DEVELOPING INDIA AS THE MOST FAVOURABLE DESITINATION FOR CLINICAL RESEARCH / DATA MANGEMENT OUTSOURCING FOR ALL PHARMACEUTICAL AND CRO INDUSTRY ACROSS THE WORLD. ABOUT US: We understand the exact requirement of the Clinical Research Industry for their need of the trained manpower as we have experience working with Clinical Research Industry since 10 years handling Clinical Trials, Clinical Data Management, SAS, Pharmacovigilance, Drug Regulatory Affairs etc. With the experience working with CRO’s, we have designed each training module focusing to expose the students practically to each task with logical exercises covering all the areas of Clinical Trials and Clinical Data Management, CDISC-SDTM and SAS. Highly experienced staffs (SME’s) from clinical research and data management industry will only will involved in training the candidates for 90 days with hands on experience on various areas of Clinical Data Management, SAS, CDISC-SDTM/ADAM. Institute of Good Clinical Practice (iGCP) provide training in two different modes like Class Room, Online-learning. UTE OF GOOD ADDRESS: INSTITUTE OF GOOD CLINICAL PRACTICE # 2ND FLOOR, ABOVE MORE SUPER MARKET, NEAR SRIPURAM COLONY BUS STOP, MOOSARAMBAGH, MALAKPET, HYDERABAD. PH:

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 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 .

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 .