Regulatory Affairs

We deliver informed advice, pragmatic services and solutions for new product and market authorizations, Health Authority submissions, post approvals, CMC and lifecycle management to help you maximize your product’s commercial potential and market success.

New Product and Market Authorization

As submission requirements are dynamic in nature and are frequently updated by HAs worldwide, the need of the hour is to track them in an uninterrupted manner

Regulatory Assessment and Intelligence

Fervor assess and identify the GAPs and make sure to minimize the possible rejections, addressing delays and accelerate the approval process throughout the product life cycle

Post-Approval Life Cycle Management

Having full proof strategy is very important and in order to overcome unnecessary delays due to rejection or delay in the approval of proposed changes

Labeling

Frevor offers end-to-end labeling services and support for global and regional labeling management, professional assistance in drafting Investigational Brochure (IB),

Regulatory Affairs

New Product and Market Authorization

Regulatory Assessment and Intelligence

Post-Approval Life Cycle Management

Labeling

let's talk

about your next project .