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Top Stories                                                                                                                                                                    Pharmaceuticals


       CSR INITIATIVE                                                                                                QUALITY ISSUES

       ABB India supports educational programmes in 148                                                              Dr. Reddy’s, Sun Pharma recall drugs in US market

       government schools in Karnataka                                                                                  Dr. Reddy’s Laboratories and Sun                                 company initiated the Class II nation-
                                                                                                                     Pharma are recalling products in the US                             wide (US) recall on June 7, 2024, the
          ABB India has announced the expan-                                                                         due to manufacturing  issues, as per                                US health regulator said. The USFDA
       sion of two educational programmes as                                                                         the latest Enforcement  Report by the                               said a US-based unit of Sun  Pharma
       part of its Corporate Social Responsibility                                                                   US Food and Drug  Administration                                    is recalling  2,088 vials  of Decitabine
       (CSR) initiatives to support inclusive and                                                                    (USFDA).                                                            for Injection  (50-mg  per vial)  due to
       equitable education. These programmes,                                                                                                                                            “cGMP deviations”. The affected lot of
       which were being run in 98 schools in                                                                            According to the report, Dr. Reddy’s                             the chemotherapy medication was pro-
       Nelamangala, will now also expand to 50                                                                       is recalling drugs  to treat insomnia   The company issued the Class III  duced at Sun Pharma’s Gujarat-based
       schools in Peenya starting this academic                                                                      and gout in the American market. New  nationwide recall on June 4 this year.  manufacturing plant. New Jersey-based
       year, reaching a total of 148 schools and                                                                     Jersey-based Dr. Reddy’s Laboratories,  As per the USFDA, a Class III recall is  Sun Pharmaceutical  Industries initi-
       around 10,000 students from Peenya and                                                                        Inc., a unit of Hyderabad-based drug  initiated in a “situation in which use of,  ated the nationwide Class II recall on
       Nelamangala.                                                                                                  major, is recalling  13,752 bottles  of  or exposure to, a violative  product is  July 2 this year. As per the USFDA, a
                                                                                                                     Eszopiclone tablets, the USFDA stated.  not likely to cause adverse health con-  Class II recall is initiated in a situation
          The STEM  Awareness and Foun-                                                                              The affected lot has been produced  sequences”.                     in which the use of, or exposure to, a
       dational Literacy and Numerical Skills                                                                        at Dr. Reddy’s Bachupally plant in                                  violative product may cause temporary
       Program is aimed at supporting young                                                                          Telangana. As per the USFDA, the drug   Dr. Reddy’s Laboratories,  Inc. is  or medically reversible adverse health
       students  with  essential  scientifi c  con-  Representatives from ABB India, Shikshana Foundation and Government of Karnataka   fi rm is recalling the affected lot due to  also recalling 20,520  units of Allopu-  consequences or where the probability
       cepts and foundational and age-appro-              at the STEM and FLN Program Inauguration                   “Failed impurities/degradation specifi -  rinol tablets in the US market due to the  of serious adverse health consequences
       priate skills in literacy and numeracy  the programme aims to equip primary  tion  with the  Centre  for  Environment   cations”.               “presence  of foreign  substance”.  The  is remote.
       alongside STEM topics. Integrated  and higher primary students with the  Education (CEE). It aims to prepare
       within the school timetable, it provides  much-needed competencies essential  higher primary school students to face   Biocon Biologics receives approval from EMA
       hands-on learning opportunities, making  for their cognitive development. Parya-  environmental sustainability challenges
       learning interactive and engaging. Run  varan Mitra, the other programme, will  by engaging them in eco-friendly activi-  to manufacture biosimilar, Bevacizumab
       in partnership with Sikshana Foundation,  be launched soon, and run in collabora-  ties in schools and its surroundings.
       LIVELIHOOD GENERATION                                                                                            Biocon Biologics, the biosimilars  EMA coordinates these  inspections  to  The facility has previously been
                                                                                                                     subsidiary of Biocon Ltd., has received  verify that a medicine manufacturer  approved to manufacture  biosimilar,
       CSIR and M.S. Swaminathan Research Foundation                                                                 approval from European Medicines  complies to these minimum standards.  Trastuzumab, in September 2022.
                                                                                                                     Agency (EMA) to manufacture biosimi-
       to focus on rural development                                                                                 lar, Bevacizumab, a type of targeted can-  Sanofi  India puts Mumbai head-
                                                                                                                     cer drug treatment at its new multi-pro-
          The  Council  of  Scientifi c  and                                  Speaking on the occasion, Dr. Kalai-    duct monoclonal antibodies (mAbs) drug   quarters on the block
       Industrial Research (CSIR) and the                                 selvi, stated that although CSIR labs      substance facility at Bengaluru.  This
       M.S. Swaminathan Research Foundation                               disseminate technologies developed in      approval  will  provide  signifi cant  addi-  French  pharmaceutical company  of other operations. In May 2023, the
       (MSSRF) have entered an MoU to work                                the labs to potential users, the outreach,   tional capacity to address patients’ needs  Sanofi ’s Indian arm has decided to put  company’s board of directors decided
       together for livelihood generation among                           especially in the societal sector, would be   across markets in Europe.      the standalone property spread  over  to demerge its consumer health business
       rural, tribal, and farming communities.                            greatly enhanced by joining hands with                                       150,000 sq ft that  houses its  country  into a separate legal entity, to allow it to
                                                                          organisations such as MSSRF that work         The company announced that EMA  headquarter  in Mumbai’s Powai loca-  have independence to pursue its growth
          The MoU was signed by Dr. N. Kalai-                             at the grassroots level. Dr. Swaminathan   has renewed its Good Manufacturing  lity on the block, a Reuters report said  strategies and this was approved by the
       selvi, Director General, CSIR and                                  stated that MSSRF is seeking select low-   Practice  (GMP)  Certifi cates  of  Com-  quoting unnamed sources.   shareholders in December. The National
       Dr. Soumya Swaminathan, Chairperson,                               cost and affordable technologies.  Tri-    pliance for its biosimilars manufactur-                             Company Law Tribunal, Mumbai, fol-
       MSSRF. Senior offi cials from CSIR and                              bals and various other such groups, she    ing facility at Bengaluru and its insulin   The company has already picked up  lowing a hearing, sanctioned the de-
       representatives of MSSRF witnessed the  across the CSIR labs and mentoring the  added, are not able to directly approach   facility in Malaysia  following routine  an  offi ce  in Vikhroli  suburb  through  a  merger in May 2024, paving the way for
       signing of the MoU.  The MoU entails  SHGs/NGOs/FPOs and other voluntary  CSIR labs due to many reasons includ-  GMP inspections. Good manufacturing  long-term lease to shift one of its divi-  the listing of the new separate company,
       creating a framework for the transfer of  organisations selected  by MSSRF  for  ing geographical location, communi-  practice describes the minimum stand-  sions Sanofi  Consumer Healthcare and  Sanofi   Consumer  Healthcare  Ltd. This
       affordable, proven and selected techno-  livelihood generation and empowerment  cation challenges  and lack  of required   ard that a medicine manufacturer must  is in the process of leasing additional  demerged entity will operate from the
       logies with societal relevance available  of women, tribal population.  resources.                            meet in their production processes. The  space for growth as well as relocation  newly leased Vikhroli offi ce premise.


       148                                                                      Chemical Weekly  July 23, 2024       Chemical Weekly  July 23, 2024                                                                  149


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