Quality & Compliance Details
This editable area is designed for quality system notes, GMP execution, registration progress, certificates, compliance documents, batch release, and drug safety information.
Certificates and Compliance Documents
Use the rich text editor in the admin panel to upload GMP certificates, production licenses, product registration approvals, compliance documents, or laboratory qualification images. You may also add certificate numbers, validity dates, issuing authorities, and applicable scope.
Quality System
Quality Is Built into Every Process
At ViengKham Pharmaceutical Co., Ltd, quality is not only the result of final testing. It is built into every stage of our daily operations, from raw material management and production control to laboratory testing, documentation, product release, and continuous improvement.
As a legally approved pharmaceutical manufacturer in Laos, the company follows GMP-based management principles and is committed to establishing a standardized, traceable, and continuously improving quality system. We understand that pharmaceutical manufacturing is directly related to public health and patient safety. Therefore, quality is always placed at the core of our production and management activities.
GMP-Based Quality Management
ViengKham Pharmaceutical Co., Ltd operates an approximately 6,000-square-meter GMP-standard manufacturing facility in Vientiane Province, Laos. The facility is designed with clear functional zoning, controlled production environments, standardized process flow, and supporting quality management procedures.
Our quality system is developed around GMP requirements and covers key areas such as personnel training, material control, production management, equipment management, cleaning procedures, laboratory testing, documentation, deviation handling, product release, and traceability management.
By implementing GMP-based procedures, we aim to ensure that each batch of products is produced under controlled conditions, recorded accurately, tested properly, and released responsibly.
Raw Material and Supplier Control
Quality control begins before production. The company manages raw and auxiliary materials through supplier qualification, material receipt inspection, storage control, status labeling, and batch traceability.
Before materials are used in production, they are checked and tested according to established quality standards. Only materials that meet the required specifications may enter the production process. This helps reduce quality risks from the source and provides a reliable foundation for stable product quality.
Controlled Production Process
During production, operators follow approved batch manufacturing records and standard operating procedures. Key production steps are monitored and reviewed to ensure that each process is carried out according to defined requirements.
The company controls important production factors such as material verification, equipment status, environmental conditions, process parameters, in-process checks, cleaning status, and production records. These controls help ensure that the manufacturing process remains stable, consistent, and traceable.
Quality Control Laboratory
ViengKham Pharmaceutical Co., Ltd has established a quality control laboratory to support raw material testing, in-process control, finished product testing, and environmental monitoring.
The laboratory is equipped with commonly used pharmaceutical testing instruments, including high-performance liquid chromatography, UV-visible spectrophotometry, dissolution testing, disintegration testing, hardness testing, friability testing, electronic balances, pH meters, drying ovens, stability chambers, microbiological testing equipment, and autoclaves.
Through laboratory testing and quality evaluation, the company ensures that products meet required quality standards before they are released to the market.
Documentation and Data Integrity
A reliable quality system depends on complete, accurate, and traceable records. ViengKham Pharmaceutical Co., Ltdimplements documentation management across production, quality control, warehouse management, equipment maintenance, cleaning, training, and product release.
Batch manufacturing records, testing records, equipment records, cleaning records, training records, material records, and release documents are managed according to internal procedures. These records allow the company to review product history, trace material sources, verify production activities, and support quality decisions.
We believe that good documentation is not only a regulatory requirement, but also an important tool for responsible pharmaceutical manufacturing.
Deviation, Investigation, and Corrective Actions
The company pays close attention to deviations, abnormalities, and potential quality risks during production and quality control activities. When a deviation occurs, it is recorded, assessed, investigated, and handled according to established procedures.
Corrective and preventive actions may be implemented when necessary to reduce the possibility of recurrence. Through this process, the company continuously improves its management system and strengthens quality risk control.
Product Release Management
Finished products are released only after production records, laboratory testing results, and quality documents have been reviewed. The quality department evaluates whether the product meets established requirements before approving release.
ViengKham Pharmaceutical Co., Ltd follows the principle that products that do not meet quality requirements must not be released. This reflects our responsibility to customers, patients, and public health.
Personnel Training and Quality Awareness
People are a critical part of the quality system. The company provides training for production, quality, warehouse, equipment, and management personnel, including GMP awareness, job responsibilities, standard operating procedures, hygiene requirements, safety requirements, and quality risk awareness.
Employees in key positions are required to receive training and assessment before performing their duties. Through continuous training, we aim to build a team that understands standards, follows procedures, and takes responsibility for quality.
Continuous Improvement
Quality management is a long-term commitment. ViengKham Pharmaceutical Co., Ltd continuously reviews and improves its quality system through daily supervision, internal checks, training, process optimization, equipment maintenance, data analysis, and management review.
We believe that stable quality comes from consistent execution, careful records, disciplined operations, and continuous improvement.
Our Quality Commitment
For ViengKham Pharmaceutical Co., Ltd, quality is the foundation of trust. We are committed to building a pharmaceutical quality system that is standardized, practical, traceable, and continuously improving.
Our commitment is clear:
To follow GMP-based management principles.
To control quality throughout the entire production process.
To ensure that every batch is properly recorded, tested, reviewed, and released.
To improve continuously through training, data, and responsible management.
Consistency is Our Innovation.
Consistency is not only our slogan. It is our daily standard, our management philosophy, and our long-term responsibility as a pharmaceutical manufacturer.
Qualifications & Compliance
VienKham treats compliance as the foundation for long-term market cooperation. The company continuously improves licensing, registration, production, quality, and distribution documentation in line with local and target-market requirements.