ENergon Labs is a Customer Focused, cGMP compliant, USFDA Inspected, ISO 9001:2015,ISO 17025:2017 Certified Analytical Testing Laboratory located at Hyderabad India, catering to Pharmaceutical, Biopharmaceutical, Medical Devices & Packaging Industries.
Our services are meticulously designed to cater to diverse client needs, & our foundation is firmly established on the principles of Integrity, Involvement, and Intelligence. You can rely on our highly qualified workforce and diligent procedures to consistently deliver data of exceptional quality that is precisely aligned to your specifications. We provide dedicated project management and technical expertise, ensuring seamless collaboration to meet project deadlines.
Analytical Method Development and Validation Services
Energon Labs can develop and validate methods for raw materials, excipients, drug substance and drug products.
Extractables and Leachables Studies
Energon Labs is a one Stop solution for testing Extractables in Container closure systems, Single-use manufacturing components
GTI & Nitrosamine Impurities Analysis
Genotoxic Impurities are chemicals that can harm by causing damage to DNA. Regulatory agencies worldwide require thorough testing for these impurities.
Elemental Impurities Analysis Services
Drug substance/ products may contain trace amounts of elemental impurities that could be harmful, even at low concentrations.
Stability and Photostability Studies
Energon Labs can support our client for execution of stability studies through well designed stability protocols, coordination for stability program
Peptide Analysis Services
Effective Characterization of peptide therapeutics at each step of manufacturing is necessary to minimize lot-to-lot variation in product quality.
In-Vitro Binding Studies Services
The BE approach is not applicable for Locally Acting Gastro Intestinal Drugs since they are not intended to be absorbed into the systemic circulation