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With our strong development and regulatory capabilities, and backed by manufacturing sites, that have over 35 regulatory body accreditations, we actively assist customers with Life Cycle management of their products. We assist our customers with:
- Improve / Manage the margins of life cycle products.
- Extent patent life by developing extensions of the current dosage forms :
- Paediatric Dosages
- Modified Release
- Simpler dosage form : Liquid from a Lyophilised form
- Improve supply chain modalities
- Improve operational efficiency
- Site Transfers
- API Source change /Additions
- Regulatory Support
- Pharmaceutical Development Services
- New Dosage form development for existing dosages
- Modified release profiles for existing IR solid dosage form
- Site Transfers: Support on Change of manufacturing sites in APIs / Formulations which needs high levels of project management services, process improvement acumen and strong focus on operational efficiencies
- API Source change / Additions: API source additions for smoothers supply chain and cost reduction
- Regulatory support
High Potency APIs (HPAPIs)
Finished Dosage Manufacturing
Late Lifecycle Management
We consider route scouting as a focused business to rapidly assist our partners in discovering and developing cost effective, competitively advantaged, robust chemical processes from early drug phase through commercial launch.
We provide our enzyme catalyzed processes for fast track discovery and development of novel, green & economical routes to APIs.
We have been providing pharmaceutical intermediate and API process development services for nearly three decades from our network of R&D and manufacturing facilities across the globe.