MPL is a leading contract manufacturing and packaging company specializing in the production of human drug products, including ANDAs, Schedule IV controlled substances, prescription, OTC, and homeopathic products, as well as animal drug products including ANADA, prescription, and OTC. Due to the wide spectrum of products produced in its facility, MPL operates its business under the drug-world umbrella to ensure the highest level of Quality Control and GXP compliance. We use the drug standard as our guide for product development, pilot batch, and scale-up, stability programs and validations, and commercial processes. The drug standard is the benchmark for all internal processes at MPL, from receipt of raw materials to release of finished product.
MPL makes its clients feel secure about putting their business in the hands of a CMO that uses the correct approach to producing drug products. Its in-house Quality Control laboratory is fully equipped with extensive analytical capabilities and is run by a highly trained staff who are prepared to perform a wide range of lab work necessary for testing drug products in all stages of development and commercialization. MPL’s drug manufacturing capabilities range from liquid to semi-solid and solid dosage forms, and its extensive filling and packaging capabilities range from manual filling operations to fully automatic, custom-built filling lines.
Drug serialization is at the forefront of our operations, from line level systems all the way through the Level 5, EPCIS. No matter how large or small the project, MPL is equipped to handle it. Our team approach is designed to control the entire process to ensure a result as precise as the product. Make sure your contract manufacturing company makes it right. Call MPL toll free today at 1-800-523-0191 or submit a New Product Request Form here.