International Pharmaceutical Trading Labs Fda& Dea Registered

International Pharmaceutical Trading Labs Fda& Dea Registered company information, Employees & Contact Information

Method development and Validation, Process Validation, and Cleaning Validation. Testing of Raw Material and Finished Product: Raw material and finished product testing for quality batch release is performed following the USP, EP, BP, JP, FCC, AOAC, and Client methods. Quantitative Assay Analysis, High-Performance Liquid Chromatography with various kinds of Detectors such as UV-Visible, Fluorescence, Photo Diode Array, Refractive Index, and Evaporating Light Scattering Detector (ELSD) Gas Chromatography with various detectors like Flame Ionization detectors (FID) and Thermal Conductivity detectors (TCD) UV-Visible spectroscopy, Structure identification High-Performance Liquid Chromatography coupled Triple Quadruple Mass Spectrometry (LC/MS/MS) Gas chromatography coupled with Mass Spectrometry (GC/MS), Infrared Spectroscopy (FT-IR), and residual solvent analysis. Gas chromatography coupled with Headspace (GC -HS) Karl –Fischer for Water determination, Refractometer, Polarimeter, Viscometer, Fluorimeter, pH meter, Melting range instrument, TLC, and Moisture Determination Balance. Metal analysis, Atomic Absorbance (AA), Graphite Furnace Atomic Absorbance, and Flame Photometer.Dissolution Testing, USP Dissolution Apparatus I (Basket) and II (Paddle), Wet Chemistry Analysis. Stability Testing, we have Experienced in all types of stability studies, from bulk drugs. Laboratory Practice (GLP): Good Analytical Skills and Good Laboratory Documentation Practices, Laboratory Safety Skills, Data integrity, and HPLC system security.cGMP for Production: cGMP of Personal Hygiene, Contamination sources, and controls. Good Documentation Practice, cGMP under controlled conditions, cGMP for Tableting and Encapsulation. cGMP for Packaging and Labeling: the Packaging Process, Primary and secondary packaging, Reconciliation Process, and Good Documentation Practice. cGMP for Sterile: cGMP under controlled conditions, cGMP for Microbiology, Good Behavior in Clean Rooms, Gowning procedure.

Company Details

Founded
-
Address
470 Chamberlain Ave,
Industry
Pharmaceutical Manufacturing
NAICS
Pharmaceutical and Medicine Manufacturing
Medicinal and Botanical Manufacturing
Pharmaceutical Preparation Manufacturing
In-Vitro Diagnostic Substance Manufacturing
Biological Product (except Diagnostic) Manufacturing
HQ
Paterson, New Jersey
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