Prominent Turnkey Project Design & Engineering Company is a group of experts having rich experience of Conceptualizing, Designing, Engineering, Project management and Qualification / Validation of various Pharmaceutical & Biotech projects. Organization is renowned Pharma consultancy providing Engineering Project Design, Project Execution, Qualification, Validation, On-going GMP compliance, Quality Assurance, Training & Internal audits services on Turnkey basis to various Pharmaceuticals & Biotech projects. Organization is offering GMP Compliant, innovative & Pragmatic solutions for a variety of services for Pharmaceutical & Biotech projects. Company has expertise in Feasibility studies and Master planning, Conceptual Design Studies, Basic Engineering, Detailed Engineering, Project Management, Procurement Assistance (TC/ TR/ Expediting), Construction Management, Commissioning Support, GMP-compliance Consulting, Qualification and Validation, Facility Audits for GMP Compliance, Energy Audits, Customized Training Services (CTS), QA Outsourcing Services, Mock Pre approval Inspectorate (by former USFDA inspectors). The company has Headquarter in Delhi with branch offices in Mumbai & Hyderabad. Company has already worked & successfully completed different types of Projects (Green Field & Brown Field projects of Solid Oral, Injectables, Liquid Oral, Lyophilized, Semi Solid Formulation, API & Bulk Drugs for different Pharma & Biotech clients like: Cipla, Lupin, AstraZeneca, Eisai Pharma, Wockhardt, Zydus Cadila, Sun Pharma, Horiba India, B.Braun Medical, Mylan, Serum Institute, Eisai Pharma, Horiba India Pvt. Ltd., Kemwell, Famy Care, ZYG Pharma, Alpa Laboratories, Sterigene Life Sciences, Richcore Lifesciences, Cosmas Research Labs, Brooks Lab, Agio Pharmaceuticals, Mitra Industries, Gufic Biosciences, Rajasthan Antibiotics, Nitin Lifesciences, Ashish Life Sciences. Company has also started its own Pharma Oncology Injectables manufacturing facility for Regulated markets at Jabalpur. Madhya Pradesh in 2015 & offering highly quality Oncology Injectables in strict compliance to international & local regulatory norms. The facility is WHO-GMP certified & also audited by EU-GMP authorities. Company is having focus to design facility to comply with USFDA, EUGMP, MHRA, WHO-Geneva, Anvisa, PICS, TGA, MOH, Invima, MCC, GCC, Schedule M & other regulatory requirements.