In the US and North America, strict compliance with the drug manufacturing regulatory guidelines laid down by the FDA is followed. This ensures safety, efficacy, and quality standards that help in the healing process. It applies to solid, semi-solid, and liquid dosages that CDMOs manufacture at their state-of-the-art plant and laboratories.

If you’re a pharmaceutical company looking for a reliable CDMO that can help in your endeavor of semi-solid dosage form manufacturing, shortlist a few accredited and certified partners. Outsource your semi-solid drug products to brands that invest heavily in R&D, and emphasize clinical trials.

Ensure, that the CDMO is in a position to obtain swift FDA approvals for clinical trials, as that can help your drug/medicine (generic or prescription) to be introduced quickly in the market.

When outsourcing your semi-solid drug product to a third party, look for their expertise, resources, infrastructure, know-how, and professionalism. As semi-solid drug forms comprise ointments, pastes, lotions, gels, chewable, foam, and sensitive topical creams, they must adhere to strict safety standards. They must 100% comply with the FDA regulations.

Therefore, you need to partner with a big and reputable CDMO brand that has the know-how to produce a semi-solid dosage by mixing it accurately under precise conditions.

Pick a CDMO based on its Expertise to Manufacture Bulk Semi-Solid Dosage Products

While shortlisting CDMO partners and third-party manufacturers, your focus should be on an entity involved in activities like API sourcing, drug formulation, analytical testing, etc. Look for a company that is into R&D, manufacturing, and packaging, apart from API procurement. This ensures partnering with a trustworthy firm that has extensive industry experience.

As you’re choosing a semi-solid dosage forms manufacturer from a list of many, focus on entities that have a global presence, apart from all over North America. Get an insight into their working procedures, manufacturing facilities, FDA approval applications, and compliance with federal regulations regarding a new product. It can be solid, liquid, or semi-solid.

Outsource to a company with a dedicated manufacturing facility spread over acres of land. Most importantly, a CDMO that possesses full-service capabilities, right from sourcing quality APIs to manufacturing finished products, is the right choice. It must be in a position to bring your semi-solid dosage/formulation into the market at the right time.

Therefore, forging a strong partnership with a reliable vendor is key to your success in the pharmaceutical industry, as your competitors are on the lookout for loopholes. Outsource smart, eliminating all bottlenecks regarding time, processes, quality, and efficacy. This is how it works!