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Preparation of DMF / ASMF / CEP dossiers as per the ICH M4 CTD/eCTD guidelines.
Preparation of response to queries raised by various regulatory agencies customer.
Preparation of Applicant s Part of ASMF as per customer requirement and restricted part of ASMF as per regulatory requirement.
Initiation of activity for timely notification / prior approval from regulatory agencies in case of any changes required to the existing DMF / ASMF / CEP on ongoing basis
Initiation preparation of renewals or revisions for CEPs / annual reports for USDMFs / ASMF variations.
Keeping update about the current global regulatory requirement
Evaluation of change control applications for regulatory implications.
Dishman is a global, dynamic group of companies offering a continuum of services to the pharmaceutical industry. We are a global outsourcing partner for pharmaceutical companies, offering a portfolio of products and development, scale-up and manufacturing services.
Job ID: 111349853