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DESCRIPTION:9TH ANNUAL PHARMA REGULATORY SUMMIT 2026\n\n&nbsp\;\n\n“Drivin
 g Regulatory Excellence for a Changing Pharma Landscape”\n\n&nbsp\;\n\n24
 th March 2026\, Hotel Kohinoor Continental\, Mumbai\, India\n\n&nbsp\;\n\
 nThe 9th Annual Pharma Regulatory Summit 2026 congregates foremost global
  pharmaceutical industry professionals and regulators to share their insi
 ghts on technologies\, approaches\, and solutions that will drive innovat
 ion and quality for the medicines delivered to patients worldwide. This i
 nteractional setting with expert-led regulatory and industry presentation
 s will ensure pharmaceutical industry professionals to develop and apply 
 ingenious solutions in today’s Indian pharma ecosystem.\n\n&nbsp\;\n\nSpo
 nsor / Delegate Registration E-mail - kavitha@virtueinsight.co.in or M: +
 91 9361957193\n\nDELEGATE REGISTRATION :\n\n&nbsp\;\n\nSuper Early Bird P
 rice (Valid until 06th Feb 2026) – INR 10\,000+ GST (18%) per delegate\n\
 n&nbsp\;\n\nEarly Bird Price (Valid from 07th Feb - 13th March 2026) – IN
 R 12\,000+ GST (18%) per delegate\n\n&nbsp\;\n\nStandard Price &nbsp\;– I
 NR 15\,000 + GST (18%) per delegate\n\n&nbsp\;\n\nSPONSORS:\n\n&nbsp\;\n\
 nConference Sponsor – Should you wish to Sponsor\, or purchase a Exhibiti
 on Stall (Booth) / paid Speaker Slot / create brand awareness\, you can s
 imply email or call your interest and queries.\n\n&nbsp\;\n\nKEY SPEAKERS
 :\n\n&nbsp\;\n\nMAYUR PARMAR\, Drugs Inspector (Deputy Collector\, Gujara
 t Government)\, FDANAGENDRAN IRUKULAPATI\, &nbsp\;Sr. Vice President – Gl
 obal Regulatory Affairs\, Aurobindo PharmaRAMANARAYANA PARHI\, Vice Presi
 dent &amp\; CIO\, Alkem Laboratories\n\nJULIET REBELLO\,&nbsp\;Director -
  Clinical Dev Strategy &amp\; Medical Writing\,CiplaANJU AGARWAL\, Direct
 or Global Patient Safety\, Advanz PharmaAMITA BHAVE\, Director Regulatory
  Affairs\, AstraZeneca\n\nMILIND ANTANI\, Leader\, Pharma and Healthcare\
 , Nishith Desai Associates\n\nPALLAVI TRIVEDI\, Associate Director – Diab
 eties and Obesity\, Global Business Services (GBS)\, Novo Nordisk&nbsp\;\
 n\nSANTOSH TAUR\, Director Medical Affairs\, Vaccines\, Rare Diseases and
  Digital\, Pfizer\n\nAKSHAYA ODAK\,&nbsp\;Head Regulatory Affairs (Biotec
 h)\, LupinPROTITI BAGCHI\, Associate Director- Digital Transformation\, G
 SKSUCHITA MORE\, Director Medical Modernization\, Asia Pacific &amp\; Jap
 an\, Merck Sharp &amp\; Dohme&nbsp\;\n\nAMARNATH SUGUMARAN\, Director - M
 edical Affairs\, Cipla&nbsp\;&nbsp\;SHUVANKAR BALLAV\, Head\, Regulatory 
 Affairs - Advanced Biotech Lab (ABL)\, Ipca LaboratoriesPANKAJ CHAUDHARI\
 , Head - Global Regulatory Affairs (Biosimilar)\, AbbottAMOL CHOULWAR\, G
 roup Leader - Regulatory Affairs (Biosimilar Peptides New Drugs Vaccines)
 \,Cipla&nbsp\;\n\nMINOO BIJU\,&nbsp\;Head-Regulatory Affairs\, Piramal Ph
 arma SolutionsMARTINA GOMES\, Head\, Reg Affairs – CH\, BayerPRIYA CHATTE
 RJEE\, Head Regulatory Affairs - South Asia\, BayerSHIRAZ KANDAWALLA\, He
 ad – Regulatory\, Quality &amp\; Safety – India\, Ferring PharmaSADANAND 
 KULKARNI\, Head - Medical\, Regulatory\, Vigilance &amp\; Quality (South 
 Asia)\, Fresenius KabiJAYASHRI PRAMOD\, Regulatory Principal Specialist\,
  Novo NordiskSUSHMITA KUSWA\, Head Medical &amp\; Regulatory Affairs\, Pi
 ramalOMPRAKASH S. SADHWANI\, Former Joint Commissioner &amp\; Controlling
  Authority\, FDA (Maharashtra State)RUCHIR SHAH\, Head Medical Devices Ca
 tegory\, Regulatory &amp\; Safety Manager\, Reckitt BenckiserRASHMI HEGDE
 \, Former Executive Vice President – Medical\, GSKNEELU GOEL\, Regulatory
  Affairs - Head Business Continuity &amp\; Compliance\, Sun PharmaPRIYA P
 RASAD\, General Manager – PV\, LupinKAVITA LAMROR\, Partner\, RWE &amp\; 
 Digital Transformation\, Maxis Clinical Sciences\n\n&nbsp\;\n\nPlus more 
 joining soon\n\n&nbsp\;\n\nFOCUS AREAS:\n\n\nDigital Transformation\nBiol
 ogics &amp\; Biosimilars\nRegulatory Writing &amp\; Submissions\nClinical
  Trials/DCT\nPatient Safety\nRWE/RWD\nNew Drugs\nGeneric Groups\nVendor M
 anagement\nMedical Devices\n\n&nbsp\;\n\n&nbsp\;WHO SHOULD ATTEND AND WHO
  YOU’LL MEET:\n\n&nbsp\;\n\nThis conference is specifically designed for 
 pharma\, biotech\, CRO’s\, Government and Regulators\, Hospitals/Trial Si
 tes\, Technology / Solution Providers from following areas\;\n\n&nbsp\;\n
 \nRegulatory Affairs\, Clinical Trials / Clinical Data\, Biologics &amp\;
  Biosimilars\, Medical Devices\, Regulatory Writing/Medical Writing/Publi
 shing/Information/Submissions\, Document and eRecords Management\, Clinic
 al Trials Management/Data\, Outsourcing /Vendor Management\, Quality Assu
 rance/Quality Control\, Technology AI\, ML\, Blockchain\, Big Data\, Supp
 ly Chain Management \, Government- Department of Health\, Vaccines R&amp\
 ;D / Innovation\, Consultants\n\n&nbsp\;\n\nGet more from the event\, wit
 h a broader scope bringing the whole communications value chain together.
  Enjoy and make the best out of our dedicated networking time\, and meet 
 the leading international vendors showcasing the products of tomorrow in 
 the co-located exhibition. Expand your knowledge of the latest business m
 odels and strategies at the high-level conference.\n\n&nbsp\;\n
DTEND:20260324T170000
DTSTAMP:20260512T214303Z
DTSTART:20260324T090000
LOCATION:Kohinoor Continental\, Andheri - Kurla Road\, Konkan Division\, 4
 00059\,
SEQUENCE:0
SUMMARY:9TH ANNUAL PHARMA REGULATORY SUMMIT 2026\n&nbsp\;\n“Driving Regula
 tory Excellence for a Changing Pharma Landscape”\n&nbsp\;\n24th March 202
 6\, Hotel K...
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