Our Services
Our Services
- New Product Dossier submissions: Finished pharmaceutical Products
- Active Ingredients : New Approval applications
- DMF writing
- Renewal application filing
- Product launching and targeting market strategy
- Queries response submissions
- Regulatory Post market surveillance
- Product development reports writing
- Post market surveillance report.
- Stability Protocol designing, Validation Protocol designing.
- Product variation filing
- Identifying Potential market and Product development
- Proof reading and writing of patients Information leaflets/SPCs
- Product layout and Art work development
- Dossier submission for medical devices
- Nutraceuticals product Authorization
- Herbal and Cosmetics products marketing authorization
- Hospital equipment authorization licensing and approvals
- Audit compliance technical support and response submissions for observations
- Site Master file submissions, arranging site audit plan and executions
- WHO Pre Qualification filing
- Tender filing for public supply, hospital supply