Sample Traceability
Samples and related testing information are identified and controlled throughout the laboratory process.
Greenetics Laboratory
Reliable testing. Quality built around your testing needs.
OUR VISION
We are committed to continuously strengthening our laboratory capability and responsibly expanding our testing scope in response to customer needs and quality expectations.
OUR STORY
A laboratory built on quality and continual improvement.
Greenetics Laboratory Co., Ltd. was established in 2022 with a commitment to develop dependable analytical testing services and a quality system aligned with internationally recognized laboratory practices.
Greenetics was created to make reliable laboratory testing more accessible and responsive to the practical needs of product owners, manufacturers and quality teams. We listen to the testing objective, review the sample and requested parameters, and provide clear guidance so customers can move forward with confidence.
Every testing process is carried out with care and follows the principles of ISO/IEC 17025, from request review and sample handling through controlled procedures, equipment management, quality control, traceability, technical review and report issuance.
Customer needs continue to shape how we develop. We strengthen staff competency, review laboratory performance and improve our systems and services so the laboratory can respond to changing products and quality expectations.
Our direction is to grow responsibly toward internationally recognized laboratory standards while making testing easier to access through clear information, practical sample guidance, convenient quotation tools and direct technical support when needed.
QUALITY & ACCREDITATION
ISO/IEC 17025:2017
Official accreditation certificate and announcement by the Thai Industrial Standards Institute (TISI).
QUALITY RECOGNITION
Department of Medical Sciences laboratory network.
Greenetics Laboratory is included in the laboratory network that passed proficiency testing for the quantification of active compounds in medical cannabis products and cannabis/hemp plants, published by the Department of Medical Sciences, Ministry of Public Health.
View the official DMSc announcement →
LABORATORY QUALITY
Quality throughout the testing process.
Controlled Procedures
Laboratory activities are performed using documented procedures and controlled records.
Equipment Control
Laboratory equipment is managed through maintenance, calibration and verification activities.
Quality Control
Quality-control activities support the validity and consistency of laboratory results.
Technical Review
Testing results are reviewed before the laboratory report is issued.
Records & Reporting
Laboratory records support traceability from sample receipt through final reporting.
TESTING CAPABILITY
Our Laboratory Capabilities
Explore the complete list of testing parameters currently available from our chemical and microbiological laboratories.
Chemical Laboratory
11 testing parametersAvailable Testing Parameters
- 01Cannabidiolic Acid (CBDA)
- 02Cannabidiol (CBD)
- 03Delta-9 Tetrahydrocannabinol (D9-THC)
- 04Delta-8 Tetrahydrocannabinol (D8-THC)
- 05Tetrahydrocannabinolic Acid (THCA-A)
- 06Cannabigerolic Acid (CBGA)
- 07Cannabigerol (CBG)
- 08Total Cannabidiol (Total CBD)
- 09Total Tetrahydrocannabinol (Total THC)
- 10Total Cannabigerol (Total CBG)
- 11Potential of Hydrogen (pH)
Microbiology Laboratory
10 testing parametersAvailable Testing Parameters
- 01Total Aerobic Plate Count
- 02Total Yeast and Mold Count
- 03Bile-Tolerant Gram-Negative Bacteria
- 04Escherichia coli
- 05Salmonella spp.
- 06Clostridium spp.
- 07Staphylococcus aureus
- 08Pseudomonas aeruginosa
- 09Candida albicans
- 10Coliform Bacteria