Trigen Laboratories
Founded in 2003, Trigen Laboratories is committed to accelerating healthcare solutions by bringing quality, affordable products to customers and patients. As a vertically-integrated generic pharmaceutical business, it supports all facets of drug development and commercialization, emphasizing quality, supply chain management, and a full suite of sales and marketing capabilities. The company aims to develop, manufacture, and distribute high-quality generic pharmaceutical products, leveraging a global network of partners.
Industries
Nr. of Employees
small (1-50)
Trigen Laboratories
Bridgewater, New Jersey, United States, North America
Products
AVO Cream Topical Emulsion
Topical emulsion formulation (prescribing information available).
Complete Natal DHA
Dietary supplement product (prescribing information available).
Complete Nate Chew
Chewable supplement product (prescribing information available).
Corvita Tablets
Oral tablet formulation (prescribing information available).
Corvita 150
Oral tablet formulation (prescribing information available).
Elite OB
Product with prescribing information (details in PI).
AVO Cream Topical Emulsion
Topical emulsion formulation (prescribing information available).
Complete Natal DHA
Dietary supplement product (prescribing information available).
Complete Nate Chew
Chewable supplement product (prescribing information available).
Corvita Tablets
Oral tablet formulation (prescribing information available).
Corvita 150
Oral tablet formulation (prescribing information available).
Elite OB
Product with prescribing information (details in PI).
Services
Strategic regulatory planning and preparation of regulatory filings and agency interactions across drug and device application types.
Internal development capabilities and partnerships to develop generic formulations and manage development programs.
Oversight of API sourcing, contract manufacturers, packaging partners and third‑party logistics to support reliable product supply.
Implementation and maintenance of quality systems and practices to meet regulatory and customer expectations.
Commercial strategy, sales operations, account management and distribution for branded and generic products.
Evaluation and execution of licensing, acquisition and partnership opportunities to grow the product portfolio.
Strategic regulatory planning and preparation of regulatory filings and agency interactions across drug and device application types.
Internal development capabilities and partnerships to develop generic formulations and manage development programs.
Oversight of API sourcing, contract manufacturers, packaging partners and third‑party logistics to support reliable product supply.
Implementation and maintenance of quality systems and practices to meet regulatory and customer expectations.
Commercial strategy, sales operations, account management and distribution for branded and generic products.
Evaluation and execution of licensing, acquisition and partnership opportunities to grow the product portfolio.
Expertise Areas
- Generic drug development
- Regulatory compliance and submissions
- Quality assurance and quality systems
- Supply chain and contract manufacturing management
Key Technologies
- Formulation development
- Regulatory submission processes (ANDA/IND/NDA/MAA/510k/PMA)
- Pharmacovigilance and REMS systems
- API sourcing and supplier management