Pepceuticals

Own products (APIs) for the generic pharmaceutical industry.

We provide quality products and services, consistently,
reliably responsibly and continuously applying some of the world’s
most difficult to handle chemical technologies.
Our independent one-site,
single entity corporate setup enables


Synthesis: Manufacturing services and products for all user industries,
using Archimica´s highly differentiated setup and technologies
APIs, Building blocks, GMP intermediates, Regulatory Starting Materials
For all global markets including the United States of America,
in total Archimica products reach 25 countries.

Procos S.p.A. is a wholly owned subsidiary of the Japanese company, CBC Co. Ltd Group, specializing in the development, scale-up and production of Active Pharmaceutical Ingredients (APIs), advanced intermediates and related services for the pharmaceutical industry.

Our core business sectors include custom synthesis and Generic API manufacturing.
The manufacturing site is located in Cameri, Italy. This 110,000 sq. meter, cutting-edge multipurpose plant, fully designed under cGMP compliance, has been successfully audited and approved by the main regulatory authorities including AIFA, FDA and PMDA.

We are a locally rooted company yet part of an international network, with commercial offices in key strategic geographies.

AltaBioscience is recognised worldwide as a leading manufacturing and analysis laboratory providing synthesis of DNA and peptides and analysis of proteins and other biochemical molecules, to researchers in academia, pharmaceuticals and the food industry.

Certified to ISO/IEC 17025:2005 for amino acid analysis, protein sequencing and steroid analysis. ISO 9001:2008 for the laboratory as a whole, AltaBioscience is committed to supplying high-quality products and analytical services at competitive prices.

• Custom Peptide Synthesis
• Tags & Conjugations
• Amino Acid Analysis
• N-Terminal Edman Protein Sequencing
• DNA/Oligo Synthesis
• Custom Antibody Generation
• Circular Dichroism analysis
• HPLC and MS Analytical Testing

ChemCon GmbH - Your Good Manufacturing Partner!
ChemCon is a contract development and manufacturing organization (CDMO) located in Freiburg, Germany. We manufacture drug substances (injectable, ophthalmic, oral, topic grade) and ultra-pure chemicals to your specifications. With multidisciplinary expertise we can meet your individual demands for small-molecule organic APIs, inorganic compounds, polymers, and highly potent or controlled substances. ChemCon’s facilities are optimized for the production of small to medium quantities (g to multi 100 kg per year). This is particularly interesting if you are sourcing APIs for clinical trials or commercial applications (i.e., orphan diseases, oncology, or emergency care) with a low annual demand. We also manufacture excipients, provocation substances, dietary trace elements, diagnostics, delivery agents, or reference standards. Your project will be under one roof from synthesis & process development/establishment all the way to commercial cGMP manufacturing, including full documentation, quality control and regulatory support. We also offer external analytical services, independent from production services. ChemCon looks back on an outstanding inspection history by both the FDA and European health authorities. Find our latest company brochure here: https://bit.ly/35ZQm8t

Impressum:
ChemCon GmbH, Engesserstr. 4b, 79108 Freiburg i.Br.
Phone.: +49 (0)761-5597-0; Fax: +49 (0)761-5597-449
E-Mail: Info@chemcon.com
CEO/President: Dr. Raphael Vogler
Commercial register: HRB 5973
Court of registration: Freiburg
VAT Reg. No: DE812753447

Chiracon GmbH has 20 years of experience in the field of drug synthesis and documentation. As a German, Berlin-Brandenburg based company the company can reliably offer all services possible in the field of synthetic drug development for new or generic products. We specialize in organic synthesis, scale up and production. Furthermore we provide all the documentation needed for active pharmaceutical ingredients (APIs) for clinical trials, and also in order to introduce new APIs to market - ASMF (active substance master files) /DMF (drug master files), Pharmaceutical Quality/CMC (Chemistry, Manufacturing and Controls) /IMPD (Investigational Medicinal Product Dossier). We utilize a management system which is based on an integrated ISO9001 system and includes a GMP environment.