Pharmaceutical Reference Standards | APIs | Impurities | Excipients | Degradation Products | NDSRIs | Working Standards | Intermediates
Mikromol helps pharmaceutical laboratories to make better, safer, medicines – by providing over 7,000 top-quality reference standards for impurities, APIs, and excipients, across more than 1,000 API families.
Most Mikromol analytical measurements are performed under its ISO/IEC 17025 scope of accreditation, with a leading range of 1,000+ standards manufactured according to ISO 17034 specifications. Each Mikromol reference standard also comes with a Certificate of Analysis that features market-leading levels of detail and transparency – enabling customers to audit by trace and mitigate risk.
Mikromol employs the most advanced techniques to characterise its standards, so that analysts can rely on the scientific integrity of the data contained in their COAs. To give laboratories even more confidence, Mikromol also uses real-time stability testing and expiry date management that ensures reference standards are received as certified, and ready for analysis.
• API standards
• Excipient standards
• Impurity standards
• Nitrosamines
• Extractables and leachables
• Pharmaceutical toxicology
• Cardiac drugs and beta blockers
• Respiratory drugs
• Analgesics
• Antibiotics
• Non-steroidal anti-inflammatory drugs (NSAIDs)
• Anticancerous
• Steroids and derivatives
• Antipsychotics
• Antidepressants
• Antihistamines
• Hormones
• Antivirals and antiretrovirals
• We enable our customers the ability to achieve higher accuracy in their analytical results in order to manufacturer better safer medicines.
• Consistently and competently deliver high quality, globally relevant pharmaceutical reference standards.
• Many certified to ISO 17034
• Certificate of Analysis that features market-leading levels of detail and transparency – enabling customers to audit by trace and mitigate risk.
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