Analytical Services
Regcure Pharma provides comprehensive pharmaceutical analytical services to support drug development, quality control, and regulatory submissions. Our analytical testing solutions include method validation, impurity profiling, residual solvent analysis, and elemental testing to ensure compliance with global regulatory standards.
Our team works with certified laboratories and validated analytical methods to deliver accurate and reliable testing results for pharmaceutical products.
Our Pharmaceutical Analytical Testing Capabilities
- Assay Method Validation (AMV) & verification for assay, dissolution & RS testing
- Residual solvent analysis
- Impurity profiling with chromatograms
- CDP development
- Elemental testing support across multiple test categories
Quality & Regulatory Compliance
All analytical testing is conducted in laboratories that follow internationally recognized quality standards. Our testing processes comply with WHO guidelines, GLP certification requirements, and ISO-accredited laboratory practices to ensure reliable and regulatory-compliant analytical results.
Advanced Analytical Instruments Used
- High Performance Liquid Chromatography (HPLC)
- Gas Chromatography (GC)
- Ultraviolet Spectroscopy (UV)
- Infrared Spectroscopy (IR)
- Thin Layer Chromatography (TLC)
- Mass Spectrometry
- Titration systems
- Sterility and BET testing systems
Importance of Analytical Testing in Pharmaceutical Development
Analytical testing plays a crucial role in ensuring the quality, safety, and efficacy of pharmaceutical products. Regulatory authorities require comprehensive analytical data during drug development and regulatory submissions.
Our analytical services help pharmaceutical companies generate reliable data for regulatory documentation, stability studies, and product quality evaluation.