Our expert team can help pharma companies increase their professional value through our advice on strategic, cost-effective, and innovative product development planning system setups for cGMP according to the world regulatory authority guidelines as well as GMP compliance. We help with plant design to GMP approval by any regulatory agency worldwide.
We also provide support by giving post submission query responses and the expert’s opinion on the same and technical advice to scale up and tech transfer projects for finished formulations, various dosage forms, and legal services.
Our consultancy services include regulatory affairs consulting, product development, and analytical and QA consulting.
Our consulting programs are designed to meet specific client requirements and we provide in-house, on-site at multiple client locations or third part facilities. We provide complete analytical program design, laboratory design & instrumentation, validation planning & design, Data envelopment analysis (DEA), clean room assessment and monitoring, on-site good manufacturing practice (GMP) / good laboratory practice (GLP) training, quality management systems, regulatory affairs, supplier qualification & on-site GMP audits and validation support.
Swaroop Tech guides our clients to grow faster and work smarter using design and operational quality approaches that suit their specific requirements and settings. This helps them improve the customer experience and business performance against the rising competition in the industry while reducing costs and maintaining the quality levels of the pharma products.
If you are looking for pharma consultancy services, get in touch with us today.