July 16, 2021
Centre for Drug Regulatory Affairs has launched a 𝗖𝗲𝗿𝘁𝗶𝗳𝗶𝗰𝗮𝘁𝗲 𝗖𝗼𝘂𝗿𝘀𝗲 𝗼𝗻 𝗚𝗲𝗻𝗲𝗿𝗶𝗰 𝗗𝗿𝘂𝗴 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗶𝗼𝗻𝘀. The course aims at providing a know-how of regulatory submission requirements for a generic drug to USFDA.
Objectives of the course:
1. Understanding the stages of regulatory control.
2. Regulatory forms and procedures of USFDA.
3. Hands-on training in Pharma Ready® an eCTD software.
4. Detailed content and requirements of USFDA form.
Duration: 15 hours
Timings: 09.30 am – 04.00 pm IST
Last Date for registration: August 1, 2021
Coordinator: Dr Krishnamurthy Bhat, Professor, Department of Pharmaceutical Quality Assurance, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal.
CLICK here to download the brochure
Quality Improvement Program entitled ‘Development and Evaluation of Biopharmaceutical Products’
Guest Lecture organized by Department of Pharmacognosy on 20th December, 2021
Dr. Jyothsna Manikkath, Assistant Professor, Department of Pharmaceutics at Manipal College of Pharmaceutical Sciences, and team publish a paper in Advanced Drug Delivery Reviews
Ms. Navya Ajitkumar Bhaskaran, Research Scholar (ICMR-SRF) bagged second prize in poster presentation session at APA India 2021
Dr Lalit Kimar and Mr Naga Thirumalesh bags second place in Grand Challenge 2021