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We offer organic and inorganic chemicals that comply with the following compendia:- United States Pharmacopeia (USP/NF)
- European Pharmacopoiea (EP)
- American Chemical Society (ACS)
- British Pharmacopoiea (BP)
- Japanese Pharmacopeia (JP)
Our pharmaceutical excipients comply with current Good Manufacturing Practices (cGMP) regulatory requirements.
Flexible solutions (customized formulas and quantities)
Since 1966, we have been providing customized solutions. Whether you need a product with unique specifications or a non-standard quantity, we can meet all of your requirements.
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| The new ACE program ensures transparency and compliance for excipients used in pharmaceutical production. |
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| Quality Control |
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Research Chemicals |
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Distribution |
- Ultrapure solvents and reactive agents
- Salts, minerals and sugars
- Acids
- Primary Standards
- Test Solutions / Buffers |
| - Excipients
- Reagents
- Fine Chemicals
- Chromatography
- Chemical intermediates |
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- Active Pharmaceutical Ingredients(API)
- Reference Standards (USP/EP/BP/JP)
- NIST
- J.T. Baker |
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Quality, Purity, Safety and Suitability for Pharmaceutical Manufacturing
ACE: A&C’s Excipient Program
Globalization of the pharmaceutical industry and the harmonization of international regulatory requirements have placed increasing demands on Pharmaceutical Manufacturers. A&C has implemented the new A&C Excipient Program called ACE. All the chemicals within ACE are specially prepared for use as components in drug product manufacturing.
cGMP
The excipients in the ACE program are manufactured with adherence to the GMP and Quality Control principles of:
- PQG - Institute of Quality Assurance's Pharmaceutical Quality Group;
- IPEC - International Pharmaceutical Excipients Council;
- WHO - World Health Organization's GMP Guidelines for Excipients;
- ISO - International Organization for Standardization.
GMP processes and documentation control begin with incoming inspection, identity and in-house testing. These records become an integral part of the documentation chain of traceability that is maintained until the final product reaches the customer. Product sampling, packaging and production take place in controlled environments with laminar flow HEPA-filtered air. A&C personnel are competent, GMP aware and GMP trained.
Change Control
Customers are notified of significant changes and pre-approval can be given. Change controls govern:
- raw materials
- packaging and sources-material specifications
- test methods
- manufacturing and analytical equipment
- production processes
- manufacturing and packaging sites
Customer Focus is Paramount
A&C engages the customer in determining the excipient quality, labelling, specifications and delivery requirements before supply commences. Skilled A&C staff support the customer’s documentation requirements by assembling all Quality documents including GMP certificates, certificates of origin, BSE/TSE and residual solvents statements and others into a standard dossier assuring completeness.
To ensure the excipients that you require are part of the ACE program, contact us. |
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