Review

• REGULATORY ENVIRONMENT FOR MEDICAL DEVICES IN NEW ZEALAND

  Akshay Anand M

  Pages 1-12

  • View PDF Abstract Download PDF DOI 10.22270/ijdra.v5i1.191
• SCALE UP AND POSTAPPROVAL CHANGES (SUPAC) GUIDANCE FOR INDUSTRY: A REGULATORY NOTE

  Mounica N.V.N., Sharmila V. Reddy, Anusha S., Evangeline L., Nagabhushanam M.V., Nagarjunareddy D., Brahmaiah B.

  Pages 13-19

  • View PDF Abstract Download PDF DOI 10.22270/ijdra.v5i1.192
• REGULATORY REQUIREMENTS OF ‘SIMILAR BIOLOGICS’ FOR MARKETING AUTHORIZATION IN INDIA

  Sharmila V. Reddy, Mounica N.V.N, Anusha S., Evangeline L., Nagabhushanam M.V., Nagarjunareddy D., Brahmaiah B.

  Pages 20-24

  • View PDF Abstract Download PDF DOI 10.22270/ijdra.v5i1.193
• UNDERSTANDING TECHNICAL BARRIERS TO TRADE AGREEMENT

  Subba Rao Bayya

  Pages 25-29

  • View PDF Abstract Download PDF DOI 10.22270/ijdra.v5i1.194
• REGULATIONS GOVERNING CLINICAL TRIALS IN INDIA, EUROPE AND USA- A COMPARATIVE STUDY

  Pooja Agarwal, Priyanka B.

  Pages 30-39

  • View PDF Abstract Download PDF DOI 10.22270/ijdra.v5i1.195