Services

1. Registration Support- New Drug Application 9/28/2011

   Our Regulatory Department has successfully assisted a number of companies with various applications to the regulatory authorities in the US, Europe and Japan.

2. Biologics Custom Manufacturing Services 1/30/2012
   DSM provides turn-key biologic manufacturing solutions, contract manufacturing for preclinical development, clinical trials or commercial supply and reduced cost, risk, and time to market.
3. Contract Development Services 1/13/2014

   Norwich offers comprehensive product development capabilities with R&D, GMP pilot scale manufacturing, analytical development and validation, and testing services. Our fully licensed facilities allow for quick and seamless transition from early stage development through clinical supplies and submission batch manufacturing.

4. Contract Manufacturing Services 1/12/2014

   Norwich offers a full range of solid dose manufacturing and packaging capabilities with flexible containment solutions for potent compounds.

5. Clinical Research Services 1/11/2014

   Norwich offers a range of clinical services to the pharmaceutical and biotech industries. Our unique combination of clinical expertise, therapeutic experience, equipment and processes means that Norwich can manage and overcome challenges with specific focus on maximizing project budgets and meeting timelines.

6. Semi-Solid & Liquid Manufacturing 1/10/2014

   DPT’s Center of Excellence for Semi-solids and Liquids is supported by in-house quality and microbiology labs, robust quality systems and a team of highly skilled technicians to support your manufacturing needs.

7. API Process Development 6/1/2012

   Cedarburg Hauser Pharmaceuticals now has the technology and experience to offer you synthetic and semi-synthetic process development as well as natural product isolation and purification.

8. Controlled Substance Manufacturing & Development 6/1/2012

   Pharmaceutical companies that are interested in outsourcing the development and manufacture of DEA controlled substances need a partner that is equipped to perform cGMP processes as well as several other levels of operational complexities. 

9. Potent Compound Development & Manufacturing 6/1/2012

   There is a continuing trend toward pharmaceutical companies developing highly active and highly targeted drugs that provide therapies for specific diseases and conditions.  Many of these drugs are potent and therefore require complex chemistry and special facility requirements during their development.  

10. Regulatory Services 6/1/2012

    If you need help preparing and submitting your API regulatory applications, Cedarburg Hauser Pharmaceuticals has the knowledge and experience it takes to efficiently guide you through the complexities of the FDA submission process.