Assist with the case processing, submission, tracking and maintenance of individual case safety report and medical device report documents involving approved products.
Assist with the processing, submission, tracking and maintenance of safety report...
- Preparation and compilation of Module 2, 3, 4 and 5 for the regulated markets (Europe/Australia/Canada) in CTD/eCTD format.
- Handling queries on Quality, Clinical, Non-clinical and Bio-equivalence parts received from the different regulatory auth...
We are looking for Customer Sales Representative for our client in pharmaceutical industry to sell their online pharma courses and trainings.
The candidate should have experience of handling and making (inbound/outbound) calls to prospective custome...
RS3,00,000 To 5,00,000Baddi, Mohali ( Chandigarh )
Strong With Regulatory Documentation
Mfr/Sop/Amv(Analytical Method Varidation),Actd/Ctd, Dossier Preparation
Having A Sound Knowledge Of Bmr Preparation And Filing, Fr&D Documentation, Pv Etc
Will Be Responsible For Handling Regulatory Affai...
Report and analayse regulatory policy
2. Interact with regulator on company issues and regulations
3. Respond to regulator on consultation papers
4. Respond to regulator on consumer complaints received from them.
Given in an opportunity to work closely within a Pharmaceutical & Biotechnology consulting company, you will be able to catalyze the organizational growth by providing regulatory in-sights for specific products for Indian market.
- Reviewing Doc From Adl, R&D, Quality & Prod.
- Life Cycle Management Through Amendments / Annual Reports.
- Managing Databases And Up-Keeping Of Recording Systems
- Preparation And Reviewing Of Regulatory Dmf.
- Response To Customer Dmf...