CSH Pharma Group

FAQs

CSH PHARMA GROUP

Frequently Asked Questions

You can contact our sales team via [email/contact form], and we’ll provide a customized quote based on your product specifications, volumes, and regulatory needs.
We assist with regulatory filings, DMFs (Drug Master Files), COAs (Certificates of Analysis), and other compliance documentation required for market approval.
We adhere to stringent containment and segregation protocols to prevent cross-contamination, ensuring safety for both patients and workers handling penicillin products.
Our state-of-the-art facilities have scalable production capabilities to meet both small-scale and large-volume demands efficiently.
Yes, we offer customized formulations, dosages, and packaging solutions tailored to client requirements, including pediatric formulations, combination drugs, and specialty antibiotics.
We follow strict quality control protocols, including microbial testing, stability studies, and environmental monitoring, to ensure sterility, potency, and safety in every batch.
Absolutely. Our facilities comply with Good Manufacturing Practices (GMP) and are regularly audited to meet FDA, EMA, WHO, and other international regulatory requirements.
We supply high-quality penicillin APIs (Active Pharmaceutical Ingredients) and finished dosage forms to pharmaceutical companies worldwide, including North America, Europe, Asia, and other regulated markets.
Yes, we provide end-to-end contract manufacturing (CMO) and packaging services for penicillin-based drugs, ensuring compliance with global regulatory standards.
CSH Pharma Group produces a wide range of penicillin-based antibiotics, including penicillin G, penicillin V, amoxicillin, ampicillin, and other beta-lactam antibiotics in various forms (tablets, capsules, injectables, and suspensions).

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