About us
Parobi Pharma-Tech is a GMP Consultancy services based in Panchkula, India.
Parobi Pharma brings in years of collective experience in the areas of a drug substance as well as a drug product development, analytical method development & transfer, technology transfer, manufacturing, quality assurance & control, regulatory affairs, pharmaceutical engineering qualification & validation and supply chain.
Our focus is on GMPs, but we cover so much more than that. We offer a broad range of services, from GMP compliance, qualification & validation, regulatory, engineering and design consulting services, Plant Design services and Training services.
We are professionals having 16+ years of experience in pharmaceutical industry across domestic and international markets. Our experience spans from small, mid-sized to multi-national companies.
We facilitate drug manufacturing companies achieve necessary regulatory approvals for their business. Our aim is to support businesses that have marketing licence but do not have EU GMP approved plants that can supply the drug products.
We value client satisfaction, integrity, honesty and confidentiality of data.
Visionis to be the leader in the delivery of Pharma Technical Services.
MissionTo contribute to our customer's success by helping them develop deeper and better understanding of technical aspects necessary for achieving GMP/ Quality compliance and manufacture quality products.
Lead Consultant
Narinder
Additionally, he has lead team of experts in preparing the regulatory filings, facing GMP inspections / audits and responding to the inspectional observations of various regulatory agencies, such as WHO, ISO, USFDA, EUGMP, MHRA, ANVISA etc.
Narinder has worked with medium to large, well respected pharmaceutical organizations like Dabur India, Unichem, Ind Swift, Panacea Biotec, Venus Remedies & Nectar Lifesciences
He is well travelled and has also worked on short and long assignments PAN India.
Lead Consultant
Dinesh
His main area of expertise is aseptic processing & areas of interests are sterility assurance, manufacturing technology, process validation, failure investigations, trouble-shooting, continuous improvement and resolution of complex technical/ regulatory/ GMP issues. Additionally, he has lead team of experts in preparing the regulatory filings, facing GMP inspections / audits and responding to the inspectional observations of various regulatory agencies, such as WHO, ISO, USFDA, UK-MHRA, ANVISA, TGA, INVIMA, MCC etc.
Dinesh has worked with various renowned organizations such as Cipla Ltd, Venus Remedies, Fresenius Kabi, Nectar Lifesciences