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Production Capabilities

Manufacturing Capabilities in a Hema pharma are where the drugs are produced, packaged, and distributed. These facilities must adhere to strict regulations and guidelines to ensure that the drugs produced are safe, effective, and of high quality.

Pharmaceutical manufacturing facilities can range from small, specialized operations to large, complex facilities that produce a wide range of drugs. Here are some of the main types of manufacturing facilities found in pharmaceutical companies:

Our capabilities include:
  • Active pharmaceutical ingredient (API) manufacturing facility: This type of facility produces the active ingredient in a drug, which is then used to make the final product. API manufacturing is typically a complex process that involves multiple steps and can take several months to complete.
  • Formulation manufacturing facility: This type of facility takes the API produced in an API manufacturing facility and turns it into a final product, such as a tablet or capsule. This process involves mixing the API with other ingredients, such as fillers, binders, and coatings.
  • Packaging and labeling facility: Once the final product is produced, it is sent to a packaging and labeling facility, where it is packaged in appropriate containers and labeled with all necessary information, such as the drug name, strength, and dosage instructions.
  • Sterile manufacturing facility: Some drugs must be produced in a sterile environment to prevent contamination. Sterile manufacturing facilities are designed to minimize the risk of contamination during the production process.
  • Quality control (QC) laboratory: QC laboratories are responsible for testing the drugs produced in the manufacturing facilities to ensure that they meet all regulatory requirements and are of high quality.