Polucon Group provides advanced pharmaceutical testing services to ensure the safety, quality, and compliance of medicines and raw materials. Our laboratory is equipped to perform comprehensive analyses, helping pharmaceutical companies, healthcare providers, and regulatory bodies meet stringent standards.
We analyze active pharmaceutical ingredients (APIs) and excipients to confirm identity, purity, and potency. Our finished product testing ensures that medicines meet regulatory specifications for safety and effectiveness.
We conduct microbiological analysis to detect microbial contamination in pharmaceuticals, ensuring compliance with Good Manufacturing Practice (GMP) and pharmacopeial standards.
Our stability testing services evaluate the impact of environmental conditions on pharmaceutical products, determining their shelf life and ensuring long-term efficacy.
Tablet and capsule dissolution testing assesses drug release properties to verify bioavailability and therapeutic efficacy.
We help pharmaceutical manufacturers comply with international and local regulations, including WHO, GMP, and KEBS standards.
Ensure the safety and quality of your pharmaceutical products with Polucon Group. Contact us at polucon@polucon.com or call +254722229944 / +254716200222 to book your service.
