Top courses
- Certificate
- Online
- Different dates available
- 4 Months
...Many countries have started adopting the eCTD standard and are accepting eCTD submission. EMEA has started accepting eCTD Submission for all centralized... Learn about: Marketing Authorization, Documentation Department, Regulatory Affairs Associates...
- Certificate
- Distance learning
- Different dates available
- 4 Months
...the fundamental and concepts of Quality Control and Assurance. It will enhance their knowledge and skills in the field of QA QC. AS a Quality control/... Learn about: Contract Research Organization, Clinical Research Organization, Medical Devices...
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20 YEARS
← | →
- Certificate
- Pune
- Different dates available
- 3 Months
...regulations and policies set by the regulatory bodies for the pre-market approval, manufacture and post-marketing compliance of medical devices... Learn about: Medical Device Manufacturers, Quality Assurance, Quality Control People...
...regulations and policies set by the regulatory bodies for the pre-market approval, manufacture and post-marketing compliance of medical devices... Learn about: Medical Device Manufacturers, Quality Assurance, Quality Control People...
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20 YEARS
← | →
- Post Graduate Diploma
- Pune
- Different dates available
...This course is designed to give industry level education in field of legal and regulatory issues. These issues are very critical to Pharma companies... Learn about: Regulatory Affairs Consultants, Drug Inspector/Drug Controller, Regulatory Affairs head/ Director...
- Post Graduate Diploma
- Pune
- Different dates available
- 6 Months
...Regulatory Affairs Assistance Regulatory Affairs head/ Director Medical Information Associates Drug Inspector/Drug Controller/ Drug Safety Specialist/... Learn about: World Affairs, Marketing Authorization, Clinical Studies...
- Certificate
- Pune
- Different dates available
- 3 Months
...Know whether document generated is adequate for your dossier submission Clarify & Comply with the regulatory requirements when submitting your dossier... Learn about: Pharmaceutical Regulations, Monoclonal Anti-Bodies, Module 3 (CMC) of Biopharmaceuticals...
Reviews on Global Institute of Regulatory Affairs (2)
Reviews
Centre rating
Recommended
Pooja Bansode
Certification Program - Medical Device Regulatory Affairs
shahid meera mohammed
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Description
GIRA Is Providing Industry oriented training and courses Since 2010. We have trained more than 500 participants so far. GIRA expertises in Pharmaceutical regulatory affairs, quality control, eCTD, Medical device, Food, and Cosmetic Industry. GIRA Is a perfect group of companies having more than 25 years experience in Pharmaceutical Consultation