GMP Practices
Documented production, equipment qualification and controlled procedures.
MEKSMAR PHARMA
Quality.
Without compromise.
Quality
QUALITY IN EVERY STEP
A quality mindset.
From the very beginning.
Consistency, documentation discipline and controlled execution support reliable delivery.
Raw materials, packaging materials and finished batches are checked through documented quality-control processes. The catalog describes equipment calibration, air validation, process validation and staff training as part of the manufacturing workflow.
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OUR QUALITY FRAMEWORK
Discipline you can build on.
Four connected areas support consistent project execution.
Chemical Analysis
HPLC, GC, UV, FTIR and TOC equipment support analytical work.
Traceability
Checks from incoming raw and packaging materials to final product release.
Microbiology
Biosafety cabinets, autoclaves, incubators, air sampling and particle counters.
STANDARDS & DOCUMENTATION
The right information
for your market.
The company catalog refers to ISO 9001, ISO 22000, ISO 13485 and GMP practices. Contact our quality team for current certificates and their applicable site and product scope. Industry reference logos do not imply membership or endorsement.
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LABORATORY STUDIES
Evidence at
every stage.
Physical and organoleptic analysis complements chemical and microbiological testing. The laboratory equipment list includes dissolution testing, densitometry, refractometry, melting-point analysis, polarimetry and microbalances.
LET’S BUILD WHAT’S NEXT
Your next idea.
A healthier tomorrow.
Bring us your vision. Let’s shape the right lozenge solution, together.
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