Toxicology analysis - Import export

INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining Eye Irritation / Eye damage hazard assessment. From standard regulatory hazard assessments to providing information on the degree of ocular irritation, to discriminating among extremely mild eye area products, INVITRO-CONNECT’ Study Monitors take the time to understand your specific goals and apply the most relevant, cost-effective strategies to achieve them. Tests for Eye Irritation / Eye damage hazard assessment in vitro: HET-CAM Assay BCOP: OECD 437 Isolated Chicken Eye Test: OECD 438 STE / Short Time Exposure (STE, OECD 491): Ocular Irritection EpiOcular & SkinEthic HCE Reconstructed human Cornea-like Epithelium (RhCE): OECD 492 For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com

INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining Eye Irritation / Eye damage hazard assessment. From standard regulatory hazard assessments to providing information on the degree of ocular irritation, to discriminating among extremely mild eye area products, INVITRO-CONNECT’ Study Monitors take the time to understand your specific goals and apply the most relevant, cost-effective strategies to achieve them. Tests for Eye Irritation / Eye damage hazard assessment in vitro: HET-CAM Assay BCOP: OECD 437 Isolated Chicken Eye Test: OECD 438 STE / Short Time Exposure (STE, OECD 491): Ocular Irritection EpiOcular & SkinEthic HCE Reconstructed human Cornea-like Epithelium (RhCE): OECD 492 For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com

INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining skin Corrosion: - OECD 435 - Skin Corrosion : "In Vitro Membrane Barrier Test Method for Skin Corrosion" (Corrositex): The Corrositex® assay is a standardized and quantitative in vitro test developed as a replacement for the dermal corrosivity rabbit test. The Corrositex® assay is presently the only in vitro assay approved by the U.S. Department of Transportation for testing potential corrosive materials and assigning packing group categories. For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com More than 80 test laboratories - Product safety - Regulatory service - In vitro tests - All OECD tests for pharmaceuticals, chemicals, medical devices and cosmetics - Study monitoring, MSDS etc.

https://www.invitro-connect.com/en - Your International Experts for Laboratory Testing and Regulatory Services - More than 80 test laboratories in our network - Product safety - Regulatory service - in vitro tests - All OECD tests for pharmaceuticals, chemicals, medical devices and cosmetics - in-house toxicologistes - Preclinical Services - Project management - Study monitoring --> complete services - all from one hand !!! --> contact@invitro-connect.com We would like to manage also your projects. Best regards Dr. Ute Hassmann (Deputy Managing Director) and Pascal Piller (Managing Director) INVITRO-CONNECT GmbH #biocides #toxicological #chemicals #laboratory #regulatory #affairs #reach #projectmanagement #pharma #medical #study #devices #Labor #GLP #cosmetics

Our experts support you with the following services: - Toxicological assessment within the framework of the REACH and biocide regulations - Environmental Risk Assessment (ERA = Environmental Impact Assessment), e.g. for pharmaceuticals - Literature research and evaluation - Examination of the reliability and validity of the studies carried out (according to OECD guidelines, EU methods or according to Klimisch et al. 1997) - Assessment of relevant toxicological endpoints, e.g. acute toxicity, genotoxicity, irritation / corrosion of the skin or eyes - Evaluation of all relevant toxicological, ecotoxicological endpoints, e.g. freshwater organisms (daphnia, algae, fish) - Read Across - Study monitoring of studies - Creation of the Endpoint Summaries and Endpoint Study Records for IUCLID (REACH and biocidal active ingredients and products) - Safety assessment and safety report for cosmetic products - Water hazard class - etc. Questions?--> contact@invitro-connect.com

INVITRO-CONNECT GmbH is your ideal partner and service provider for your projects in the field of life science for chemicals / REACH, pharmaceuticals, biocides, cosmetics and medical devices. We are the strong partner at your side who provides our tailor-made service modules according to your project requirements. You have the choice to individually select the modules that you urgently need in your projects from our modular service system. With our technical expertise and our customer-oriented approach, we fit in perfectly with your projects and processes, so that we form a team and nothing stands in the way of the project's success. The Modules can be individually and flexibly adapted for each project. For more information please contact INVITRO-CONNECT GmbH. INVITRO-CONNECT GmbH - Your International Experts for Laboratory Testing and Regulatory Services Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com

- in vitro gene mutation study in bacteria: Ames Test OECD 471 - in vitro gene mutation study in mammalian cells: Mouse Lymphoma Assay (MLTK Assay) OECD 490 - in vitro gene mutation study in mammalian cells: HPRT test / OECD 476 - Micronucleus Assay in vitro (Human Lymphocytes or V79 cells) / OECD 487 - Chromosomal aberration Assay in vitro (Human Lymphocytes or V79 cells) / OECD 473 - Hen’s Egg Test – Induction of Micronuclei (HET-MN) - COMET Assay in different cell types - Cell Transformation Assay in Bhas Cells / OECD 231 (draft) - Mammalian Erythrocyte Micronucleus Test / OECD 474 / ISO 10993-3 - Combined Mammalian Erythrocyte Micronucleus Test with concurrent Alkaline Comet Assay in vivo OECD 474 & 489 - In vivo Mammalian Alkaline Comet Assay / OECD 489 - Unscheduled DNA synthesis (UDS) Test with Mammalian Liver Cells in vivo / OECD 486 - Mammalian Spermatogonial Chromosomal Aberration test / OECD 483 - Mammalian Bone Marrow Chromosomal Aberration test / OECD 475

- OECD 439 / Skin Irritation Test (SIT) in a Reconstructed Human Epidermis (RhE) Model - Skin Irritation in the regulatory hazard classification and labeling context is defined as the production of reversible damage to skin following a defined chemical exposure. The Skin Irritation Test (SIT) is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing moderate skin irritation (UN GHS Category 2 Skin Irritants1), and to discriminate UN GHS Category 2 Skin Irritants from UN GHS 3 Mild Skin Irritants as well as those not requiring classification for skin irritation potential. INVITRO-CONNECT GmbH has extensive expertise with a wide variety of reconstructed skin-based protocols. For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com

- OECD 431 - Human Skin Corrosion: "In Vitro OECD 431: Reconstructed Human Epidermis Test Method, in vitro Test - Skin Corrosion in the regulatory hazard classification and labeling context is defined as the production of irreversible damage to skin, generally evident as necrosis through the epidermis and into the dermis, following a defined chemical exposure. The In Vitro Skin Corrosion Test is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing skin corrosion (UN GHS Category 11), and in some cases to partially subcategorize corrosives into UN GHS Sub-Categories 1A or 1B and 1C (ie., the current test methods do not effectively discriminate between UN GHS Sub-Categories 1B and 1C). For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com

There are two types of Vitamin D. Vitamin D2 (ergocalciferol) is obtained from food. It is metabolized by liver to its active form 25 hydroxycalciferol [25 OHD2]. Vitamin D3 (cholecalciferol) is synthesized in skin by sunlight's UV rays. It is metabolized by liver to 25 dihydroxycalciferol [25 OH D3] is involved in many biochemical functions including calcium and bone metabolism regulation. Vitamin D deficiency is associated with Ricketts, osteomalacia, depression and impaired cognitive function. Elevated Vitamin D levels decrease depression. High-dose vitamin D3 is also used to prolong remission intervals in multiple sclerosis (MS) patients.

Many toxicological specimens are whole blood. This control confirms a method's accuracy for quantitating heavy metals associated with poisoning in whole blood.

Trace elements are essential compounds necessary for a wide variety biochemical reactions including oxidation-reduction, synthetic and metabolic processes. They are a required cofactor for many enzymes. Trace element deficiencies associated with a failure of those enzyme systems for which the element serves as a cofactor cause biological system failures and death. Trace element toxicity is associated with overdose, usually secondary to taking too much high dose trace element supplements.

Our 100% Real Whole Blood is collected in FDA-licensed facilities within the United States from healthy adult donors. We screen our whole blood for common drugs of abuse and alcohol. Our frozen blank whole blood is suitable for all testing methods, including LCMS, LC-MS/MS, GCMS, Time of Flight (TOF), ELISA, EMIT and other immunoassays. This product uses Potassium Oxalate as an anticoagulant and Sodium Fluoride for preservation.

A validity control, which contains common adulterants, is utilized in drugs of abuse (DOA) testing to confirm a laboratory's DOA analytical systems are performing accurately and can identify adulterated urine specimens. Validity Controls Level 1 through 5 are used as quality control materials to help identify substituted, diluted, and adulterated urine samples. The matrices for this QC are prepared from distilled water. The levels of the Adulterants, Creatinine, Specific Gravity, and pH are adjusted to the desired range for each lot prepared. Quality control before, during, and after the preparation of the control material ensures that each lot is comparable and of the same high quality. The listed ranges were verified by analytical methods similar to those actually used in a testing laboratory.

Our 100% Real Human Urine is collected from healthy donors within the United States. We screen our urine for the following analytes: d-Amphetamine, d-Methamphetamine, Benzoylecgonine (BE), (-)-Cotinine, Morphine, Oxazepam, and (l)-9-Carboxy-11-nor-Delta-9-THC (THC-COOH). Our liquid urine contains Sodium Azide for preservation and is suitable for all testing methods, including LCMS, LC-MS/MS, GCMS, Time of Flight (TOF), ELISA, EMIT and other immunoassays.

Immunosuppressants are essential for successful organ transplants. Their drug concentrations must be routinely monitored to ensure optimal levels and patient compliance. Lower concentrations lead to transplant rejection; higher concentrations lead to severe adverse effects including Graft vs Host Disease.

Our 100% Real Normal Human Serum is collected in FDA-licensed facilities within the United States from healthy adult donors. We screen our Normal Human Serum for common drugs of abuse and alcohol. Our frozen serum is suitable for all testing methods, including LCMS, LC-MS/MS, GCMS, Time of Flight (TOF), ELISA, EMIT and other immunoassays. This product uses Potassium Oxalate as an anticoagulant and Sodium Fluoride for preservation.

Anticonvulsant, or anti-epileptic drugs, are used to treat a wide range of symptoms affecting the nervous system. Most commonly they are utilized to control convulsive seizures, psychotic behavior and pain. Many of these drugs have very narrow therapeutic ranges and low thresholds for toxicity, meaning precision and accuracy are of the utmost importance. Our serum controls for anticonvulsants are an integral part of quality control for any lab that performs therapeutic drug monitoring.

Determination of skin sensitization potential is a critical endpoint in the safety assessment of raw materials, chemicals, mixtures and formulations. Although the Guinea Pig Maximization Test (GPMT) and Local Lymph node assay (LLNA) have historically been used to address this adverse effect, in vitro assays have been developed and validated in order to replace these resource-intensive animal tests. INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining skin sensitization: - Direct Peptide Reactivity Activation Assay (DPRA, OECD 442C) - ARE-Nrf2 Luciferase Keratinocyte Activation Test Method (OECD 442D) -Human Cell Line Activation Test (h-CLAT, OECD 442E) -Kinetic Direct Peptide Reactivity Assay (kDPRA) -Myeloid U937 Skin Sensitization Test (MUSST / U-SENS) -and more Fast Project Execution: personal - competent - reliable --> contact@invitro-connect. - More than 80 Test Laboratories - Product Safety - Regulatory Service -