Active Pharmaceutical Ingredients
ACIC's API Division offers a wide range of bulk products through our Open World Network.
Please note that this list is by no means exhaustive and many of these products are in various stages of development. We invite you to contact us about these or any other products you may be interested in.
ACIC manufactures, supplies and sources, on an exclusive basis, an extensive range of Active Pharmaceutical Ingredients from cGMP and FDA inspected manufacturers.
Everyone knows the path from molecule to market. The challenge is to find the fastest and most efficient way, worldwide. The ACIC approach is designed to help you arrive at the most efficient solutions by offering you a wider range of global choices.
ACIC has helped many different leading active ingredient manufacturers to gain access to world markets – especially the hard to penetrate U.S., Canadian, European, and Latin American markets.
ACIC can provide manufacturing partners with first-class sales and product representation, regulatory approval management, and DMF / eDMF / PR-DMF as well as NDA, ANDA (USA) and C.N.O.R. (Canada) and European documentation preparation including ongoing strategic marketing advice.
ACIC has experience and resources for:
- Marketing and Sales
- Site Transfer
- Sales & Acquisition of Facilities
- Electronic CTD Format
- Regulatory Submission
- Regulatory Interpretation
- Patent Applications
- Marketing and Sales
Some of the key Therapeutic Categories where ACIC is most active in:
- Oncology Biosimilars and Pharmaceutical API's
- Protease Inhibitors
- Anti-diabetic Biosimilars and Pharmaceutical API's
Custom Manufacturing & Outsourcing Capabilities
ACIC can facilitate in all stages of API development. Ask ACIC for help with opportunity identification and validation, process development, scale-up, and commercialization. At any given time, our partner companies have many products in development that can be made available to customers at an early stage.
ACIC’s extensive experience in the synthesis of Active Pharmaceutical Ingredients is coupled with wide capability range in over 25 US-FDA inspected plants and other plants in the process of obtaining approvals. Our experience in building plants (three), streamlining plants for FDA inspection and organizing R&D groups (four), along with our extremely close working relationships with these facilities, allows us the flexibility to manufacture almost any kind of fine chemicals. (Fermentation, Synthesis, Extraction).
Since 1973, we have accumulated an international experience in the following areas of both Synthesis & Fermentation:
- Process Research
- Process Development
- Analytical Development
- Clinical Quantities under GMP and validated
- Pilot Scale-Up
- Process Optimization
- Production Validation
- Regulatory Support
- Manufacturing Scale-up and Industrial Production
Our intimate knowledge of the strengths and weaknesses of each partner plant enables us to select the best site for manufacturing. Partnering with us enables you to have the utmost flexibility and efficiency, from grams to tonnage.
ACIC offers a wide variety of customizations through its Global Network. This list is by no means exhaustive and we invite you to contact us about any other custom manufacturing requirements you may have in the areas of Custom Organic Synthesis & Fermentation.
Need more information? Feel free to contact us to get the information you need.