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Solas Certification Standards
We meet regulatory and international agency audits to ensure that each product is safe, effective and consistent.
9
Active Certification
Covers prescription drugs, OTC, cosmetics, and supplements.
24/7
Compliance Monitoring
QA and QC ensure standards are executed without interruption.
+50
Audit Team
QA/QC professionals with national & global certifications.
PT. Solas Langgeng Sejahtera implements an integrated pharmaceutical, health and cosmetics management system. Every production, storage and distribution procedure is documented and audited to ensure consistent quality.
Apart from complying with CPOB, we implement Good Manufacturing Practice, ISO and supply chain security policies. Digital documentation makes it easy to track batches and audit readiness whenever needed.
Management System
CPOB & GMP
Drug and cosmetic production standards follow BPOM and international certification.
ISO & Quality Audit
Internal-external audit processes ensure SOP compliance across all sites.
Digital Documentation
Batch tracking and electronic records facilitate quality traceability.
Official Documents
All certificates are issued by authorized institutions and renewed according to the validity period. Contact us if you require special legalization or verification.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Medicine Manufacturing Practices (CPOB) for formulation, filling and secondary packaging activities for non-betalactam oral liquid preparations, both non-antibiotics and antibiotics, in accordance with BPOM provisions.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Traditional Medicine Manufacturing Practices (CPOTB) for the production of capsule preparations, with a validity period of up to 6 May 2029.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Traditional Medicine Manufacturing Practices (CPOTB) for the production of internal medicinal liquid preparations, with a validity period of up to 19 September 2028.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Medicine Manufacturing Practices (CPOB) for the production of penicillin antibiotic tablets and its derivatives in the Betalactam Production Building, with a validity period from 22 May 2025 to 21 May 2030.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Medicine Manufacturing Practices (CPOB) for the production, formulation, filling and secondary packaging of oral powder preparations of the antibiotic penicillin and its derivatives in accordance with BPOM regulations.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the Good Manufacturing Practices (CPOB) requirements for the production of non-betalactam tablets, including non-antibiotics and non-betalactam antibiotics in the Non-Betalactam Production Building, with a validity period from 8 May 2024 to 30 April 2029.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Medicine Manufacturing Practices (CPOB) for formulation, filling and secondary packaging of non-betalactam semisolid preparations in the form of ointments, creams and gels, both non-antibiotic and antibiotic, in accordance with BPOM regulations.
This certificate states that PT Solas Langgeng Sejahtera has fulfilled the requirements for Good Medicine Manufacturing Practices (CPOB) for formulation, filling, and primary and secondary packaging of non-betalactam hard capsules, both non-antibiotics and antibiotics, with the exception of contraceptive preparations, other sex hormones, and cytostatics in accordance with BPOM provisions.
CPOB & Compliance
The Good Medicine Manufacturing Practices (CPOB) system provides guidance for the pharmaceutical industry to ensure product quality, safety and efficacy. Solas applies CPOB throughout the production line from process validation, raw material testing, to batch quality assurance.
Quarterly internal audits
The QA team performs cross-departmental checks to ensure every procedure is carried out.
Digital batch records
Electronic documentation makes tracking and inspection readiness easier at any time.
Compliance Journey
2003
Initial CPOB implementation for prescription drug lines.
2012
Certification expansion to cosmetic and supplement products.
2018
Integration of digital documentation and unified audit systems.
Now
Collaboration with international institutions for advanced certification.
Indonesia
English