Who We Are
Our thoughts and ideas revolve around 'Innovation'. We're this way- Since always! We build solutions that exceed the quality criterion and deliver the performance that furnishes every arising need of modern day industries with sheer perfection.
Process Master Technologies is an eminent name in the business sphere, renowned to offer unsurpassed IT software solutions in the field of business process management, business analytics and enterprise mobility. Evoking innovation in true sense, we aim to bring never seen before transformation in contemporary work environments to accelerate organizational progression and maximize profitability. From ideation and conceptualization to development, deployment, and after-sales services, our genius professionals know their work well and never hesitate to walk an extra mile to cater to the industry specific needs of our clients. We deliver smart, dedicated and timely services to add value in our client's business and our ISO 9001:2008 certification accredits our performance and dependable work ethics.
We aim to bring the innovation revolution- we want our clients to grow, succeed and know what being a market leader feels like. Our mission is to deliver world class IT tools and dependable services that can effectively transform the conventional business methodologies, resulting in higher productivity, greater efficiency and simplified work flow.
Our vision too is crafted clearly- to empower organizations all over the world by streamlining their business processes using the latest developments in Information Technology.
Red Lotus Pharmtech is a Pharma Technical Services company. Red Lotus Pharmtech brings in year of collective experience in the areas of drug substance as well as drug product development, analytical method development & transfer, technology transfer, manufacturing, quality assurance & control, regulatory affairs, pharmaceutical engineering qualification and validation.
KVS Technologies is a Pharma Validation services provider. KVS Technologies is promoted and managed by Mr. Kalpesh Kumar Vaghela who having 18 years of experience in Pharma validation services like PLC Software Validation, ERP Software Validation, Computer System Validation, 21 CFR Part 11 Compliance Training. KVS Technologies associated with India’s most leading pharma companies for better quality management system, and training on Gamp 5.
Manish Bhatkar is an experienced pharma professional, diligent in his core functional area (pharmaceutical technical operations) and committed to the profession. Before founding Red Lotus in 2016, in his 25 years of service, he has discharged executive as well as leadership responsibilities in the areas of design & development, manufacturing, qualification & validation, operations management, quality assurance, quality management, audits & compliance, regulatory affairs, technology transfer, project management, and technical consulting. He has worked in R&D, API's, formulations and technical consulting environments and has demonstrated equivalent capabilities in managing manufacturing, technical as well as quality operations with ease.
He is a postgraduate in Pharmaceutical Sciences and an active member of professional associations like ISPE, PDA, and IPA. In addition to being a pharma-professional, he is also a regular speaker in industry & academia seminars/ conferences and a trainer on the topics like qualification and validation, process validation, quality systems etc. He is well travelled and has also worked on short and long international assignments particularly in the UK, USA & Japan.
Deepak Dey is an experienced Pharma professional, diligent in his core functional area (pharmaceutical operations) and committed to the profession. In his 35 years (approx.) of service, before superannuating from Fresenius Kabi Oncology Limited in 2016, he has discharged executive as well as leadership responsibilities in the areas of research & development / technology transfer, pharmaceutical manufacturing, plant operations management, quality assurance, quality management, audits & compliance, and quality system automation.
He is a post-graduate in pharmaceutical science and an active member of professional associations like PDA and IPA. In addition to being a pharma -professional, he is also a regular speaker in industry and academia seminars/conferences and a trainer on the topics like pharmaceutical process, quality systems, GxP Quality Systems, 21 CFR Part 11, Gamp 5 etc.