Turning Compliance into Confidence: The Power of Biological Indicators
Biological indicators are essential tools for validating sterilization processes in pharmaceutical manufacturing. By using highly resistant microbial spores, BIs provide […]
Biological indicators are essential tools for validating sterilization processes in pharmaceutical manufacturing. By using highly resistant microbial spores, BIs provide […]
Optimize your ELISA coating by choosing the right plate, using a consistent antigen concentration and buffer, and blocking thoroughly to
“Visual inspection of injection‑molded parts is a critical safeguard in manufacturing. By detecting surface defects, dimensional inconsistencies, or contamination, early
Not all glass defects are equal. Recognizing breakage patterns, star cracks, delamination, or stress fractures, can reveal root causes and
While cosmetic defects like scratches, air bubbles, or minor glass imperfections may not compromise sterility or efficacy, they can still
FDA 483s often stem from poor inspection practices.Syrviatek’s test sets and qualification programs empower your team to detect defects with
Certified irregular particles offer a powerful edge in test set creation ensuring realistic defect simulation, inspector qualification consistency, and regulatory
Difficult-to-inspect pharmaceutical products—like lyophilized drugs, suspensions, and opaque solutions—pose major challenges for visual inspection due to their complex formats and
In today’s pharmaceutical and biotech industries, compliance isn’t optional—it’s essential. From injectable drug production to diagnostic testing, every detail matters.
At Syrviatek Laboratories, we pride ourselves on delivering low lead times without compromising quality. From our FDA-certified, ISO 9001-certified facility