July 13th, 2020 by aveciapharma
Pharmaceuticals are undoubtedly an extremely R&D intensive when compared to most other industries. As the process of producing new drugs is not only a time-consuming and costly endeavor but also has deadlines to meet. That’s why when presented with these challenges, pharmaceutical companies seek the best of the best for pharmaceutical development. That’s why they choose Avecia Pharma Services for R&D when it comes to fulfilling those urgent demands for new and more efficient medications.
For the nearly 30 years that Avecia has been around, we have garnered a reputation for providing outstanding analytical testing from small molecules to biologics in pharmaceutical development. You won’t find anyone else who provides a multitude of services at the same level of quality that we offer. Here are just some of our high-quality scientific solutions offering:
Analytical chemistry has been critical since the early days of chemistry, providing methods for determining which elements and chemicals are present in the object in question. The assurance of the quality, safety, and efficacy of new medicines this provides, has made it invaluable for pharmaceutical development. Our affordable analytical chemistry support covers compendial testing according to USP/NF, EP, BP, JP, and ACS. We also cover customer-specified monographs in support of raw materials, in-process analysis, and finished product release testing.
Developing pharmaceuticals depends upon the extensive data acquired from microbiological testing, however, it can be a timing consuming process. As examining microorganisms to ensure sterility, investigating antimicrobial effectiveness, microbial contamination, or bioburden, or analyzing endotoxins related to the manufacturing of pharmaceuticals is anything but simple. You need our microbiology team's expertise, dedicated project management, and high-quality reports. We can ensure the timeliness of that your project needs when you use our microbiological testing service.
The FDA requires that "Drug product containers and closures shall not be reactive, additive, or absorptive to alter the safety, identity, strength, quality or purity of the drug beyond the official or established requirements…". This necessitates the need to determine its impurity profile, which in turn means that the components used in the manufacture and storage of that product must be assessed. That’s where our more than 50 years of combined experience within identifying the threat of contamination from polymers, metals, and an array of pharmaceutical products comes into play. As our service is the best option for getting the purity of your pharmaceutical goods finalized for release into the market.
Avecia Pharma Services is the go-to choice for pharmaceutical companies R&D needs, as our years of experience and quality services provided by our state-of-the-art manufacturing facility can't be beaten. We can cover any of your needs with our wide array of services, and ensure all the work is done in time for any deadlines you have. Contact us today and get the best of the best in pharmaceutical research & development working on your products today.
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