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Pharmaceuticals


       PLI SCHEME
       Potassium clavulanate fermentation unit begins

       commercial production


          India’s  fi rst  unit  to  produce  the  rently met by imports from China and  tion on stamp duty and registration fee,
       active  pharmaceutical  ingredient  (API),  Korea.                 besides  subsidised  land  at  the  rate  of
       potassium clavulanate, has commenced                               Re 1 per sq.m. The centrally-funded PLI
       large-scale  production  in  the  last  few   The  state-level  Single  Window  programme was launched for the pro-
       weeks.                            Clearance  and  Monitoring  Authority  motion  of  domestic  manufacturing  of
                                         had  approved  the  project  in  its  17th  critical key starting materials (KSMs)/
          Set  up  under  the  centrally-spon-  meeting on July 7, 2021. The in-princi-  drug  intermediates  and  APIs  in  the
       sored  Production  Linked  Incentive  pal  approval  for  setting  up  the  plant  country few years ago. It was launched
       (PLI) scheme, this fermentation plant  was issued on July 28 the same year.  after  wide-ranging  deliberations  on
       at  Plassra  in  Nalagarh  (Himachal                               India’s dependence on critical resources,
       Pradesh)  unit  has  a  capacity  to  pro-  The  unit  has  also  benefi tted  from  a  risk  to  supply  chain  bottlenecks
       duce  400-tpa  of  potassium  clavula-  several  special  incentives.  These  after COVID pandemic disrupted supply
       nate.  The  domestic  demand  of  the  include 100% exemption on electricity  chains. The government had identifi ed
       API  is  pegged  at  700  tonnes  per  duty for fi ve years, 15% rebate on energy  48 critical APIs for local manufacturing
       annum, and the entire demand is  cur-  charges  for  fi ve  years,  100%  exemp-  in its fi rst initiative.

       FOCUS ON SUSTAINABILITY
       Piramal Pharma’s GHG commitment validated

       and approved by SBTi


          Piramal  Pharma  has  embarked  on  ing with global climate                 United  Nations  Global
       its sustainability journey as the Science  action goals. To further            Compact  (UNGC),
       Based Targets initiative (SBTi) offi cially  reinforce  our  commit-            World  Resources  Insti-
       validated  the  company’s  near-term  ment,  we  are  also  in                 tute  (WRI)  and  World
       greenhouse gas (GHG) emission reduc-  the  process  of  deve-                  Wildlife  Fund  (WWF),
       tion targets.                     loping a comprehensive                       guides  companies  in
                                         Carbon Reduction Plan, which will be  reducing their GHG emissions. It pro-
          The company has committed to re-  unveiled soon. While we have come a  vides a clear pathway for future-proof
       duce absolute scope 1 and 2 GHG emis-  long  way,  in  many  respects,  our  sus-  growth  by  specifying  how  much  and
       sions 42% by FY2030 from a FY2022  tainability  journey  is  just  beginning.”  how quickly emissions must be cut to
       base  year.  Piramal  Pharma  has  also  The  SBTi,  a  collaboration  between  limit  global  warming  to  well  below
       committed to reduce absolute scope 3  the Carbon Disclosure Project (CDP),  1.5°C above pre-industrial levels.
       GHG emissions from purchased goods
       and  services,  fuel  and  energy  related   USFDA completes inspection at
       activities,  upstream  transportation  and
       distribution  and  use  of  sold  products   Dr. Reddy’s Bachupally R&D centre
       25% within the same timeframe. This
       makes  Piramal  Pharma  the  third  global   Dr.  Reddy’s  Labs  has  informed  The  inspection  was  conducted  from
       pharmaceutical  company  in  India  to  that  the  USFDA  has  completed  a  September 16-20, 2024. Dr. Reddy’s
       receive  approval  from  the  SBTi.  routine  Good  Manufacturing  Practice  had  earlier  received  the  Establish-
       Ms. Nandini Piramal, Chairperson, Piramal  (GMP) inspection at its R&D centre  ment  Inspection  Report  (EIR)  from
       Pharma, said, “The approval from SBTi  (Integrated  Product  Development  the  USFDA  for  the  formulations
       reinforces our ongoing commitment to  Organisation or IPDO) in Bachupally,  manufacturing  facility  (FTO-3)  in
       reducing our GHG emissions and align-  Hyderabad  with  zero  observations.  Bachupally.

       Chemical Weekly  October 1, 2024                                                                145


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