Would you like to join our e-newsletter to be informed immediately about healthy news?
Pharmananda provides contract manufacturing services for tablets, capsules, ointments, creams, gels, vaccines and injections, ampoules. We audit the facilities and plants to ensure that they comply with the FDA CGMP requirements as specified by the norms of international regulatory agencies such as the FDA (USA), Health Canada, the MCA (UK), EDQM and EMEA (EU), the TGA (Australia), the MCC (South Africa) and the WHO.
We prepare the pharmaceutical suppliers/contract manufacturing facilities to face pre-approval inspections. We assist with inputs in responding to deficiency letters, if any, until approval is achieved. We also oversee post-approval manufacturing activities to ensure regulatory compliance and product quality.
Working with Pharmananda as your pharmaceutical export company and medical supplier, your business will benefit the following advantages:
• State-of-the art facilities, which adhere to stringent specifications of US FDA / UK MHRA approved facilities, WHO cGMP, TGA-Australia, and MCC-South Africa approved facilities.
• Qualified and experienced technical team in the areas of manufacturing, quality control, quality assurance, and development for all range of products.
• Reliable supply of quality products
• Private label manufacturing.
We integrate perfectly into your pharmaceutical supply chain to by offering a wide range of benefits to your company.