Drug Regulatory Affairs

**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...

1. 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 with fare knowledge about Food...

**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...

Job Title:Regulatory Affairs SpecialistLocation:Okhla Phase-1, Delhi-110020Department:Regulatory AffairsReports To:Head of Quality & RegulatoryEmployment Type:Full-TimeJob Summary:We are seeking a detail-oriented and knowledgeableRegulatory Affairs Specialistto ensure our medical devices comply with all regulatory requirements in domestic and international...

This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications**: Regulatory Documentation, Regulatory Requirements, and...

Job Context:To support MIBG I-131 clinical programs and other JDI innovative products in the pipeline, The Regulatory Specialist will be reporting to the director of Regulatory Affairs and support the development of regulatory strategies related to JDI clinical programs, marketing applications in US and Canada and post-marketing activities.Challenges:3....

**Company Description** Technoledge is an educational institution located in Noida. Our primary objective is to provide support for the development, coordination, implementation, and planning of educational programs. We offer a wide range of services including smart hybrid schools, engineering services, manpower solutions, skill development, e-learning...

**Role Description** This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications** - Regulatory Documentation,...