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Regulatory Affairs Certificate Course Training At Navi Mumbai

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Panvel City, Panvel

Course ID: 14820

Panvel City, Panvel

Students Interested 7 (Seats Left 0)

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Date and Time

Not decided yet.

About vishalakshi Naik

25 Years in pharma Industry
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About the Course

We are focused on Industry integrated training in Clinical Research. Centre for Clinical Research and Training Pvt. Ltd.(CCRT), Mumbai specialises in custom-designed educational courses and professional training programs for Pharma & Medical field, and has the reputation of providing the best possible training.?

We also have Clinical Research Services division at present working on phase 4 trials end to end services.

Quality Solutions is our Pharma consultancy division. Where we serve pharma & cosmetics companies to upgrade their facilities to international standards by consulting them to upgrade systems , training their staff & updating their documentation.
04.10.14

Topics Covered

Regulatory Affairs Course, Training, Certificate Course, At Navi Mumbai.
Conducted by CCRT, Mumbai at New Panvel.

Course Duration: Faculty Interaction 33hrs & Practical study 34hrs
Course Level: With Practical Assignments, 100% Industry Working Faculty,
COURSE CONTENT: -
• GMP, Quality Assurance, GLP
• Method, Process & Cleaning Validations
• Deviation management, CAPA
• CTD & e CTD, Dossier
• Audits & Inspections by Different Regulatory agencies
• Regulatory Compliance for WHO & ICH Guidelines
• Regulations for Pharma Research
• TQM – Concepts & Execution

Eligibility: Undergraduates, Graduates and Post Graduates in Science, Pharmacy, Medicine, Nursing, Management, Practicing and Working Doctors, Pharma Executives.

Who should attend

Undergraduates, Graduates and Post Graduates in Science, Pharmacy, Medicine, Nursing, Management, Practicing and Working Doctors, Pharma Executives.

Pre-requisites

Undergraduates, Graduates and Post Graduates in Science, Pharmacy, Medicine, Nursing, Management, Practicing and Working Doctors, Pharma Executives.

What you need to bring

Laptop,Notebook pen etc."

Key Takeaways

• GMP, Quality Assurance, GLP
• Method, Process & Cleaning Validations
• Deviation management, CAPA
• CTD & e CTD, Dossier
• Audits & Inspections by Different Regulatory agencies
• Regulatory Compliance for WHO & ICH Guidelines
• Regulations for Pharma Research
• TQM – Concepts & Execution

Reviews

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Discussions (1)

Students Interested 7 (Seats Left 0)

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