Drug Regulatory Affairs Executive

**Description** Drug Regulatory Affairs - Job description - Prepare CTD, ACTD Dossiers and file regulatory submissions. - Perform assessments of new or revised products. - Manage complaint documentation (including investigation and closure). - Respond to inquiries from regulatory bodies. - Should be technically well versed with requirements for medicines...

1. Drug Regulatory Affairs - Job descriptionPrepare CTD, ACTD Dossiers and file regulatory submissionsPerform assessments of new or revised productsManage complaint documentation (including investigation andclosure)Respond to inquiries from regulatory bodiesShould be technically well versed with requirements for Medicineswith fare knowledge about Food...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**About Company** **Pharma Regulatory Institute (PRI)** This is a project (PRI) of Accredited Consultants Pvt. Ltd. (ACPL), Noida who are very well established in the business of Regulatory Affairs and Pharmacovigilance for the last 25 years and created a very strong image in the industry. ACPL clients are widely distributed in Foods, Pharmaceuticals,...

**JOB POSTING FOLDER -INDEED** - **Drug Regulatory Affairs - Job description**: - Prepare CTD, and ACTD Dossiers and file regulatory submissions - Perform assessments of new or revised products - Manage complaint documentation (including investigation and - closure) - Respond to inquiries from regulatory bodies - Should be technically well versed with...

Company DescriptionTrishul Biotech is dedicated to advancing scientific research to enhance agricultural sustainability and productivity. Utilizing cutting-edge crop solutions, the company aims to improve agricultural quality with its unique Upcrop Research, Development, and Commercialization platform. This innovation has led to the production of impactful...

Job Description: - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market. - Review of technical...

Job Description:We are looking for a Regulatory Affairs Sales Executive (Fresher) who will be responsible for driving sales in the regulatory compliance sector. This role is ideal for candidates from pharmaceutical and biotech backgrounds who want to explore a career in sales and client handling within the regulatory domain. Key Responsibilities: Understand...