 ABOUT US:
Darshan Singh is a professional pharmaceutical blogger from India having long experience of 20 years in the pharmaceutical field. He completed his Master of Science in Chemistry in 2003 from Kurukshetra University Kurukshetra.
He started his job in a pharmaceutical company as an assistant QC chemist in October 2003. He joined various regulatory audits including WHO-GMP, and UK-MHRA during his first job tenure. He learned things with a passion that help him later on in his carrier.
He worked in various positions in Cure Quick Pharmaceutical, Combitic Global Caplet Pvt Ltd, and Digital Vision.
He started writing in the form of blogs article on different online platforms about the pharmaceutical industry in 2012. He got a rich experience in Quality Control, Quality Assurance, Regulatory Affairs, and Manufacturing in the pharmaceutical industry. He quit his job in July 2015 and started Laafon Galaxy Pharmaceuticals a pharma marketing company, then he started his website [LAAFON.COM] to provide technical information about core issues in the pharmaceutical industry.
He also started providing consultancy for the setup of pharmaceutical formulations plants in all dosage forms, cosmetic plants, Herbal plants, and FSSAI plants.
Usually, he covers pharmaceutical-related topics including cGMP, SOPs, MFRs, Regulatory compliance documents, DPCO, pharma plant setup guidelines, WHO-GMP, USFDA, and MHRA audits.
During his working period in different pharmaceutical companies, his core field of work was different in different companies. His working expertise and experience are provided as:
- Assistant Quality Control Chemist (2003) in Cure Quick Pharmaceuticals and Combitic Global, his responsibilities were to carry out analysis of Raw materials and Finished products with the help of chemical testings, UV-Visible Spectrophotometers, HPLC, Karl Fischer, Dissolution Tester, Autoclave, and FTIR. He used to operate all instruments in the quality control laboratory. He also used to perform chemical testing of raw materials and finished by various methods like aqueous and non-aqueous titrations. His responsibilities also include standardizing different volumetric solutions. Preparation of reagents for different chemical and instrumental tests.
- He also used to prepare documentation related to QC like COA, calibration of instruments, standardization of reagents, Validation of instruments, Validation of analytical process, preparation of SOPs, quality checkups in the manufacturing area, in-process testings, and self-inspection in the company.
- Quality Assurance Manager (2009) in Digital Vision his working responsibilities were changed along with existing duties, including Regulatory affairs jobs, Product Permission, labeling of pharmaceutical products, Review of SOPs, review of MFR, Site Master File, plant audits, compliance of cGMP norms, and product quality check-ups.Â
- He started giving consultancy services before 2015 for pharma plant design, plant setup, Layout map, regulatory compliance documents, SOPs, plant audits, etc. In the last 8 years, he has been provided consultancy for more than 30 pharma plants for plant setup.
- He also helps manufacturing chemists in developing Master Formula Records (MFRs) for different products including tablets, capsules, liquid orals, injectable dry and liquid, ointments, etc. His role remains to establish a product formula that complies with pharmacopoeial parameters like dissolution, disintegration, and assays.
His core passion is writing on pharma topics, which helps his followers. He has a large following and numerous daily readers in the pharmaceutical sector. He shares the expertise he has gained through experience with pharmaceutical experts to develop their understanding and careers in the pharmaceutical industry.
He regularly updates his website with current updates in the pharmaceutical industry. He also provides technical help to pharma professionals working in different companies in various positions. Thousands of his followers ask their questions on different social media platforms and he provides them with solutions as soon as possible.
Follow him on Facebook, Instagram, Twitter, LinkedIn, and Youtube.
ABOUT LAAFON GALAXY PHARMACEUTICALS
Laafon Galaxy Pharmaceuticals was established in 2012 by Mr. Pankaj Dhaka as a third-party manufacturing service provider. In 2012, the company provides only liaisoning services for helping pharma companies to get products manufactured in Himachal Pradesh.
Later on in 2015, Mr. Darshan Singh joined the company as a managing partner. The company deal in the marketing of pharmaceutical products, provide consultation for setting up a pharmaceutical plant, help to buy and sell running pharma plant, and consults for every regulatory job for a pharma company.
The company provides third-party manufacturing services for people who are not able to get timely services from manufacturers. We assure time-bound and high-quality product manufacturing from Himachal Pradesh and Uttarakhand.
For more inquiries, you can call or WhatsApp us on 9812446733