OVER 18 YEARS EXPERIENCE
ADMIX PHARMA LABORATORIES, LLC
CONTRACT TESTING & PRODUCT DEVELOPMENT SERVICES
Meet Admix Pharma Laboratories
FEI # 3012552148
FDA and DEA inspected
Contract Testing and Product Development
With Admix Pharma Laboratories you will enjoy a host of attractive benefits that can effectively extend your in-house pharmaceutical, nutraceutical, or cosmetic products development and analytical testing capabilities for long and short term projects. You will quickly realize how efficiently you can relieve the internal workload of your laboratory and products development department. In addition, you have our commitment to meet all agreed-upon delivery dates.
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You'll find that Admix Pharma Laboratories offers a full range of technologically advanced services. You can choose the specific services that offer the most appropriate solutions to all your needs.
Why Admix Pharma Laboratories?
At Admix Pharma Laboratories we know the path to get your company the desired end-result you are seeking. Our staff has spent over a decade honing the skills necessary to find the best ways to develop and test your future products and provide our clients with unmatched industry knowledge.
Analytical Site Capabilities
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Active Pharmaceutical Ingredients Testing
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Inactive Pharmaceutical Ingredients/Excipients Testing
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Liquid, Solid, and Semi-Solid Dosage Forms Products Testing
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Stability Testing
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Analytical Method Development and Validation
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Cleaning Validation Testing
Product Development Site Capabilities
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Liquid, Solid and Semi-Solid Dosage Forms Product Development
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Active Pharmaceutical Ingredients Sourcing
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Inactive Pharmaceutical Ingredients/Excipients Sourcing
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Product Marketability Evaluation
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Pilot Batches Manufacturing and Stability Evaluation
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Stability Indicating Analytical Testing Method Development and Validation
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Submission (ANDA)/Stability Batch Manufacturing, Testing, and Stability Evaluation
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Identification/Selection/Evaluation of an Appropriate CRO for Performance of Bioequivalence Studies
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Bioequivalence Studies Performance Monitoring
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Bioequivalence Studies Reports Evaluation
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Compiling ANDA Submissions
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Electronic Submission of ANDA (e-CTD format)
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Pre-marketing Process Validation
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Commercial Scale Manufacturing
Additional Controlled Substances Class V through I Capabilities
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Testing and developing of the products containing Controlled Substances Class I through V, including Cannabinoid products.
Services
Made in the USA and Dedicated to Excellence
Since 2003
The Quality You Can Trust
Our 100% in-process quality assurance guarantees that you will receive timely and accurate services and products.
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This unwavering commitment to quality ensures strict compliance with critical cGMP, cGLP, and cGCP standards.
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Want to work together? Send us an e-mail
Contact Info
Feel free to call anytime you have a question or concern. You always have access to the Chief Technical Affairs Officer.
Phone
Address
Office 908.546.1505
Fax 908.546.1502
3001 Hadley Road
Unit 8 South
Plainfield, NJ 07080
