Jordi Labs chemists are accustomed to working within a range of regulatory frameworks to satisfy the needs of our customers. We offer contract testing services to businesses and researchers in a wide range of market segments, which requires a holistic understanding of various certifications and standards. This promotes confidence in the reliability and quality of our results. Jordi Labs is ISO/IEC 17025:2017 accredited (PJLA, Accreditation # 96418) for chemical testing. Our ISO-accredited testing services guarantee consistency and quality in a wide range of challenging sectors.
The International Organization for Standardization (ISO) is an independent organization responsible for numerous world-class specifications that govern the quality, safety, and efficiency in various sector-specific services. Although ISO certified testing is essential for a practically limitless range of markets, sector-specific standards exist for the likes of testing and calibration laboratories.
At Jordi Labs, we are part of the ISO family, but we have also expanded our scope to ensure we satisfy a wide range of regulatory requirements. Currently, we are registered to ISO 9001:2015 and ISO/ILAC 17025:2017 (PJLA, Certificate Number L20-371, Accreditation Number 96418, for chemical testing) and we offer testing services compliant with current Good Manufacturing Practice (cGMP) regulations when required. Please contact a member of the team today with any questions about our regulatory testing services.
| Standard | Category | Description |
|---|---|---|
| ISO 1133 | ISO | Plastics -- Determination of the melt mass-flow rate (MFR) and melt volume-flow rate (MVR) of thermoplastics -- Part 2: Method for materials sensitive to time-temperature history and/or moisture |
| ISO 11443 | ISO | Plastics -- Determination of the fluidity of plastics using capillary and slit-die rheometers |
| ISO 178 | ISO | Plastics -- Determination of flexural properties |
| ISO 180 | ISO | Plastics -- Determination of Izod impact strength |
| ISO 4892-2 | ISO | Plastics -- Methods of exposure to laboratory light sources -- Part 2: Xenon-arc lamps |
| ISO 527 | ISO | Plastics -- Determination of tensile properties -- Part 1: General principles |
| ISO 307 | ISO | Plastics -- Polyamides -- Determination of Viscosity Number |
| ISO 1628-1 | ISO | Plastics — Determination of the viscosity of polymers in dilute solution using capillary viscometers — |
| ISO 6427 | ISO | Plastics -- Determination of matter extractable by organic solvents (conventional methods) |
| ISO 8536-4 | ISO | Infusion equipment for medical use — Part 4: Infusion sets for single use, gravity feed |
| ISO 11357 | ISO | Plastics – Differential scanning calorimetry (DSC) Part 1:General principles (ISO 11357-1 : 1997) |
| ISO 11979-2 | ISO | Ophthalmic implants — Intraocular lenses —Part 2: Optical properties and test methods |
| ISO 11979-5 | ISO | Ophthalmic implants — Intraocular lenses — Part 5: Biocompatibility |
| ISO 16000-6 | ISO | Indoor air — Part 6: Determination of volatile organic compounds in indoor and test chamber air by active sampling on Tenax TAâ sorbent, thermal desorption and gas chromatography using MS or MS-FID |
| ISO 16014-4 | ISO | Plastics — Determination of average molecular mass and molecular mass distribution of polymers using size-exclusion chromatography —Part 4: High-temperature method |
| ISO 18562-3 | ISO | Biocompatibility evaluation of breathing gas pathways in healthcare applications —Part 3: Tests for emissions of volatile organic compounds (VOCs) |
| ISO 29941 | ISO | Condoms -- Determination of Nitrosamines Migrating from Natural Rubber Latex Condoms |
| ISO 7864 | ISO | Sterile hypodermic needles for single use — Requirements and test methods |
| ISO 9626 | ISO | Stainless steel needle tubing for the manufacture of medical devices — Requirements and test methods |
| ISO 20795-1 | ISO | Dentistry — Base polymers —Part 1: Denture base polymers |
| ISO 1183-3 | ISO | Plastics — Methods for determining thedensity of non-cellular plastics —Part 3:Gas pyknometer method |
| ISO 10993-9 | ISO | Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
| ISO 10993-12 | ISO | Biological evaluation of medical devices —Part 12: Sample preparation and reference materials |
| ISO 10993-13 | ISO | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices |
| ISO 10993-17 | ISO | Biological evaluation of medical devices —Part 17: Establishment of allowable limits for leachable substances |
| ISO 10993-18 | ISO | Biological evaluation of medical devices — Part 18: Chemical characterization of materials |
| ISO 3960 | ISO | Radiometer analytical iodometric titration metod (ISO 3960) |
| ISO 11040-5 | ISO | Preilled syringes —Part 5: Plunger stoppers for injectables |
