STILLMEADOW, Inc. – Drug Development, Toxicology, Animal Health
STILLMEADOW, Inc. specializes in GLP analytical studies.
We are an independent GLP analytical studies contract research facility. We are AAALAC Accredited and certified with the National Environmental Laboratory Accreditation Program (NELAP).
Our GLP analytical studies specialists have provided full-service, lab-certified evaluations since 1975 in the areas of drug development, mammalian and environmental toxicology, animal health, entomology, analytical services, and in vitro studies.
We were certified by the Japanese Ministry of Agriculture, Forestry and Fisheries (JMAFF) in 1992. In addition, key members of our GLP analytical studies staff are members of the Society of Quality Assurance, the Chemical Producers and Distributors Association, and the Society of Toxicology.
The GLP analytical studies Quality Assurance Unit (QAU) at STILLMEADOW, Inc. assures regulatory compliance by auditing studies, reviewing protocols, Standard Operating Procedures (SOPs), consulting with study directors, and interacting with sponsors. The QAU conducts regulatory training classes, hosts regulatory as well as sponsor inspections, and assesses subcontractor compliance.
The Quality Assurance Unit carries out report and data audits, facility inspections, and in-process inspections for compliance with:
Our staff are members of the following associations:
Council of Producers & Distributors of Agrotechnology
Society of Environmental Toxicology and Chemistry (SETAC)
Association for Assessment and Accreditation of Laboratory Animal Care International
And other associations and organizations.
For drug development, FDA approval of your Investigational New Drug (IND) application is the result of a successful drug development program, which begins with STILLMEADOW, Inc.
From guidance in the creation of unique pilot studies and protocols, to evaluation of the safety and efficacy of your product, STILLMEADOW, Inc.’s experienced study directors and laboratory technicians support your drug development in meeting FDA guidelines for advancement to clinical trials.
STILLMEADOW, Inc. performs pre-clinical safety and efficacy studies, pharmacokinetic studies, and ADME (adsorption, distribution, metabolism and excretion) studies.
For Toxicology in Mammals, Avian, Fish, Reptiles and Insects: Considerable legislation has been developed to protect people and the environment from possible harmful effects of chemicals biopesticides, pharmaceuticals, and microbial pest control agents (MPCA’s). Acute and subchronic toxicity testing protocols provide fundamental data for evaluating products to inform both manufacturers and the public of potential hazards. Industries of significant economic and societal importance rely on safe use of effective chemicals for a multitude of useful and beneficial purposes. STILLMEADOW, Inc. takes pride in its ability to provide the toxicology services needed for premanufacture notification, registration of pesticides, labeling and safe handling recommendations for consumers and employees.
For Animal Health we specialize in companion and farm animals.
Our Analytical Services include:
To report an Animal Welfare concern click on this link and submit the form.
Our GLP analytical studies corporate headquarters are in Sugar Land, Texas, southwest of Houston. With 3 buildings and more than 75,000 square feet of space, we have the capacity to conduct many types of studies concurrently and hope to partner with you soon.
Contact us now for your GLP analytical studies needs!
Our GLP analytical studies facility has the most up to date equipment.