International Regulatory Affairs
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Product Specifications
| Service Type | Regulatory Affairs |
| Submission Type | CTD, DMF |
| Industry Compliance | Global Standards |
| Audit Support | Mock Audits |
| Documentation | Comprehensive |
| Training | Available |
| Usage | Drug master file, validation, training and documentation, mock audits, replies to deficiency letters, CTD preparation, making all systems adhering to IR requirements and submission of dossiers for various countries |
| Features | Regulatory Expertise, Dossier Submission, Compliance Support, Cost-Effective, Global Reach |
Company Details
Welcome to Prism Consultancy Prism Consultancy is well positioned to make the most of the global industry’s shift towards Asian market especially Indian from the erstwhile traditional markets across the globe. This is a reflection of our core strengths in innovative research & development and cost-effective production. We have the firm belief that we can add value to clients’ business. Established with a broad based product portfolio, Prism Consultancy offers Certified Contract Manufacturing Services in association with internationally approved and acclaimed BE/BA study partners, provides expertise in the International Regulatory Affairs documentation & site variations, and out lic
Business Type
Service Provider
Employee Count
10
Establishment
2008
Working Days
Monday To Sunday
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Seller Details
Ahmedabad, Gujarat
Accepts only Domestic inquiries
Proprietor
Mr. Manojit Pathak
Address
1006, Dev Prime Corporate Offices, Corporate Office makarba Road, Near Vodafone Office, Makarba Ahmedabad, Gujarat, 380015, India
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