Advanced Post Graduate Diploma in Drug Regulatory Affairs, Ipr & Patents

Modules - 1 Drug Regulatory Affairs

Modules - 2 Essential Intellectual Property and Patent Management

Study Mode

eLearning - Live Sessions

Duration

6 Months

Certificate

Cliniminds - USA ACCRE Accredited

Faculty

Fulltime Cliniminds Faculty & Visiting Experts from the Industry

Accreditation

Accreditation Council for Clinical Research Education, USA

Methodology

Live eLearning Sessions, eBooks, Audio Video Recordings and other content using Cliniminds Learning Management System.

Examination

Online MCQ / Descriptive / Project

Study Material

Access to Cliniminds Learning Management System 24x7 – Recordings, PPT, Notes, Modules, eBooks.

Placements

Extensive Placement Support. Pre Placement Training, Pitching CVs with Recruiters and assistance in arranging Interviews with the companies.

Eligibility

B.Pharmacy, M.Pharmacy, Pharm.D, Nursing, BSC, MSC, B.Tech Biotech, M.Tech Biotech, BDS, MDS, BHMS, BAMS, BPT, MBBS, all professionals working with Pharmaceutical companies, CROs and Life Sciences Consulting Firms

Entry-Level Positions:

• Regulatory Affairs Associate/Coordinator (Responsibilities: Assisting with regulatory submissions, maintaining regulatory files, ensuring compliance with regulations).
• Regulatory Affairs Specialist (Responsibilities: Preparing and submitting regulatory documents, interacting with regulatory agencies, supporting product development teams).

Mid-Level Positions:

• Senior Regulatory Affairs Specialist (Responsibilities: Leading regulatory submissions, developing regulatory strategies, mentoring junior staff).
• Regulatory Affairs Manager (Responsibilities: Managing regulatory projects, coordinating with cross-functional teams, overseeing regulatory compliance).

Senior-Level Positions:

• Regulatory Affairs Director (Responsibilities: Directing regulatory activities, formulating regulatory strategies, ensuring regulatory compliance across the organization).
• Senior Director/VP of Regulatory Affairs (Responsibilities: Overseeing all regulatory affairs activities, setting strategic direction, liaising with top regulatory bodies).

Specialized/Executive Positions:

• Chief Regulatory Officer (Responsibilities: Providing executive leadership in regulatory affairs, shaping regulatory policies, representing the organization at the highest levels.
• Consultant/Advisor in Regulatory Affairs (Responsibilities: Offering expert advice on regulatory strategies, helping organizations navigate complex regulatory landscapes).

Key Recruiters

Pfizer, Johnson & Johnson, Novartis, Roche, Merck, Sanofi, GlaxoSmithKline (GSK), AstraZeneca, Eli Lilly, Abbott, Bayer, Bristol-Myers Squibb, Amgen, Takeda, Boehringer Ingelheim, Teva Pharmaceuticals, Genentech, Novo Nordisk, Allergan, Biogen, Dr. Reddy's Laboratories, Cipla, Sun Pharmaceutical Industries, Biocon, Glenmark Pharmaceuticals, Lupin, Wockhardt, Cadila Healthcare (Zydus Cadila), Torrent Pharmaceuticals, Aurobindo Pharma, Alkem Laboratories, Jubilant Life Sciences, Piramal Enterprises, Natco Pharma, Intas Pharmaceuticals, Hetero Drugs, Alembic Pharmaceuticals, Strides Pharma Science, Freyr, IQVIA, PAREXEL, Covance, ICON plc, Syneos Health, Charles River Laboratories, Medpace, PRA Health Sciences, Pharmalex, Kinapse

Course Calender

Please contact counsellor for upcoming batch details 91 812 910 0876 / 91 484 421 6666 / 1800 1023 566 (Toll Free)

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