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      寧波亞川生物醫藥有限公司
      行業動態
      喜訊:寧波亞川注冊團隊新增一名國際審計官 廣大藥企的審計福音來啦!

      喜訊:寧波亞川注冊團隊新增一名國際審計官

      廣大藥企的審計福音來啦!

      中國藥企又,叒,叕被FDA貼出警告信啦!

      日前,FDA官網掛出對浙江一藥企的警告信,FDA評論其對缺陷的回復“草率”并未對檢查期間發現的任何缺陷給予充分的糾正措施。

      質量體系如何合規?現場審計不會應對,官方信不會回復,缺陷糾正不會開展!不用怕,寧波亞川來幫您!

      廣大藥企的審計福音來啦!

      我司專家團隊新增印度審計官之一:Sarang Athavale博士,100+家審計經驗,100+場專業培訓經驗,31+年實驗室工廠工作經驗,為您解決審計認證中的一切難題。

      Dr. Sarang Athavale

      Sarang Athavale 博士

      Quality & GMP Auditor/質量&GMP審計官

      OVERVIEW

      • Experience of 31 + years in various capacities in Quality Management, Quality Assurance, Quality Control & Sterile Manufacturing.

      31年以上豐富工作經驗,涵蓋質量管理、質量保障、質量控制及無菌生產等方面。

      • Successful experience of 100+ audits.

      成功指導過100多家藥企通過審計。

      • Successful experience of 100+ professional  trainings .

      成功開展過 100多場專業培訓會議

      • Presently a Senior Quality Advisor to many pharmaceutical companies

      目前身兼數家藥物公司高級質量顧問

       

      CORE STRENGTHS AND CORE COMPETENCE

      關鍵優勢及關鍵競爭力

      • Design and implementation of Quality Systems of international standards in pharma companies.

      根據國際標準設計藥廠質量體系、協助完成體系建立并在過程中提供解決方案。

      • Documentation of complete factory in dual language(Chinese & English).

      中英文工廠文件編制。

      • GMP Audits of API , Intermediates and Formulation facilities.

      原料藥、中間體及制劑工廠的GMP審計。

      • GMP training in Quality Systems, Validation and Qualification, General GMP, GLP, ICH guidelines.

      關于質量體系、驗證與確認、GMP/GLP/ICH指導原則等方面的GMP專業培訓

      • Successfully faced several regulated market audits – USFDA, MHRA, EU GMP , MCC,  ANVISA , GCC & others.

      成功應對許多國際審計,如USFDA/MHRA/EU GMP/MCC/ANVISA/GCC等。

      • Special exposure in handling of Sterile ( Injectables ) facilities.

      無菌(注射劑)設備的特殊暴露處理

      • Project documentation

      項目文件

      • Preparation for Pre FDA audits.

      FDA預審計

      • Develop software for QMS.

          開發QMS 軟件

      EDUCATION

      Master of Science – Biochemistry, Marathwada University, India [1985]

      理科碩士 — 生物化學,Marathwada 大學,印度[1985]

      Master of Business Administration, Marathwada University, India [1988]

      商務管理碩士  Marathwada 大學,印度[1988]

      Master of Science - Quality Management, Birla Institute of Technology and Science, India [2001]

      理科碩士 —  質量管理,Birla科技學院,印度[2001]

      Ph.D. - Quality Management Systems , Kingslake University, USA [2014]

      博士 — 質量管理系統,Kingslake大學,美國[2014]

      QUALITY SYSTEMS / GMP AUDITS

      質量系統/GMP審計

      • Preparation and implementation of Quality Manual encompassing international GMP guidelines and updating SOP documentation.Established Quality Assurance and Quality Control functions at API and Formulations including sterile manufacturing.Specially expert in Change Control System , Deviations handling , Investigations of incidents , Batch Review and Approval, Market complaints handling, Product recalls and Training to all for cGMP.

          起草與執行質量手冊,涵蓋國際GMP指導原則與更新SOP文件。為原料藥和制劑公司(包括無菌生產)制定質量保障與質量控制功能,特別擅長處理變更控制系統,偏差處理,事件調查、批審核與批準,市場投訴處理、產品召回問題和進行cGMP培訓。     

      • Faced more than 100 audits as Lead In-charge of  USFDA, MHRA, MCC, TGA, AFSSAPS, ANVISA , GCC, and WHO Geneva certification. All were successfully granted without critical observations.Conducted API audits for clients from USA , Germany , Spain and UK. International clients are GSK, Sanofi, Merck , Abbott & Pfizer.Chinese clients are Shouguang Fukang Pharma Co. Ltd, Reyoung pharmaceuticals, Singclean Medical Products Co. Ltd.

         作為主負責人參與100家以上的審計并成功通過,涉及有USFDA, MHRA, MCC, TGA, AFSSAPS, ANVISA , GCC和 WHO認證。其中指導過美國、德國、西班牙和英國客戶的原料藥審計,合作過的國際公司有葛蘭素史克、賽諾菲、默克、雅培和輝瑞;中國客戶有壽光富康藥業有限公司、瑞陽藥業有限公司、杭州Singclean 藥業有限公司。

      • Conducted more than 100 training sessions for Operators , Executives & Senior Managers on Quality Culture of Compliance as per GMP norms with Ranbaxy and many more Companies.

          開展超過100場針對操作者,高管和高級經理人關于質量合規性的培訓性會議。

      • Undergone ‘Know How’ training for medical grade PVC in Solvay Draka ,NETHERLAND for quality requirements for a sterile manufacturing facility of specialized drug products.

          參與了在荷蘭開展的關于特殊藥物產品的無菌生產設備質量要求培訓

        Few of the API Companies audited are as follows :

          合作過的原料藥公司如下:

      Granules India Ltd. , Dr. Reddy’s Labs Ltd., Cadila Pharmaceuticals Ltd., Neuland Labs Ltd., IPCA Labs Ltd., Amoli Organics Ltd. , Parabolic Drugs Ltd., Natco Ltd. , Synthochem Labs Ltd., Sami Labs Ltd., Geetanjali Chemicals Pvt. Ltd., Hetero Drus Ltd., Pearls Organics Ltd. , Wockhardt Ltd., Atul Industries , Supriya Life Sciences Ltd., Matrix Labs Ltd. , SMS Pharma ( Oncology ) , Sharp Mint Ltd. and many more …

       

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