Adnène Bouderbala

CEO at Farmavans
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Contact Information
Location
Tunisia, TN
Languages
  • Arabe Native or bilingual proficiency
  • Français Native or bilingual proficiency
  • English Full professional proficiency

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Experience

    • Tunisia
    • Wellness and Fitness Services
    • 1 - 100 Employee
    • CEO
      • Mar 2012 - Present

      Company founder Overall project management: - Financial monitoring - Manufacturing area development - Suppliers contact and raw material order Recruiting, training and development of staff Company founder Overall project management: - Financial monitoring - Manufacturing area development - Suppliers contact and raw material order Recruiting, training and development of staff

    • Resident Pharmacist
      • Nov 2011 - Jun 2012

      - Preformulation, formulation of generics - Application of a new method of preformulation (SEDEM method) - Development and validation of assays and stability indicator method - Scale-up and pilot batch manufacturing - Manufacturing process validation - Preparation of the Marketing Authorization Application (CTD format) - Supervision of pharmacy interns in training in the laboratory. - Preformulation, formulation of generics - Application of a new method of preformulation (SEDEM method) - Development and validation of assays and stability indicator method - Scale-up and pilot batch manufacturing - Manufacturing process validation - Preparation of the Marketing Authorization Application (CTD format) - Supervision of pharmacy interns in training in the laboratory.

    • Resident Pharmacist
      • May 2011 - Nov 2011

      - Daily Validation of sterilization cycles and traceability control - Management of the sterilization process under the responsibility of the pharmacist responsible for the sterilization sector - Participation in continuous quality improvement (development of policy quality of service, management of non-compliant MD, implementation of preventive and corrective measures, evaluation of customer satisfaction (OR of UH and other hospitals), updating procedures and work instruction) - Monthly monitoring of hemodialysis water and updating the control procedure - Environmental Monitoring and updating control procedures - Validation of parenteral nutrition prescriptions, preparation and control of nutrition bags (one week / month) - Night guard (provision of emergency drugs, clinical trials, preparation of parenteral nutrition bags) - Technicians and pharmacy interns training Show less

    • Resident Pharmacist
      • Nov 2010 - May 2011

      - Daily Validation of sterilization cycles and traceability control - Analysis of daily records of non-compliance and implementation of corrective actions - Update procedures - Implementation of internal and external audits - Environmental control - Study of the profitability in case of outsourcing sterilization in a private company. - Traceability of implantable MD and monthly monitoring of stocks and implementation of different notebooks care. - Technical assessment of consumables for sterilization - Toxicology: drug dosage (one week per month) - Night guard (provision of emergency drugs, clinical trials, preparation of chemotherapy bags, clinical trial management and drug dosage) - Technicians and pharmacy interns training Show less

    • Resident Pharmacist
      • Nov 2009 - Nov 2010

      - Validation of chemotherapy prescriptions (CHEMO ® software), organization of chemotherapy bags preparation, preparation of chemotherapy bags using a negative pressure pharmaceutical isolator, validation of finished preparations. - Daily management of non-compliance and implementation of corrective actions - Environmental control - Management of subcontractors - Management of clinical trials - Update procedures - Qualification of an external unit for manufacturing chemotherapy bags Show less

    • Resident Pharmacist
      • Mar 2009 - Nov 2009

      - Control of raw materials, packaging components, intermediate products and finished products and their release - Evaluation of assay methods and procedures and proposal of amendment to the development department. - Development of a stability indicating Method of levomepromazine - Control of raw materials, packaging components, intermediate products and finished products and their release - Evaluation of assay methods and procedures and proposal of amendment to the development department. - Development of a stability indicating Method of levomepromazine

    • Resident Pharmacist
      • Sep 2008 - Mar 2009

      - Daily Activity: technicians aid in various manufacturing tasks that allowed me to acquire a good knowledge of various manufacturing processes drugs. - Ensure implementation of production programs and procedures in accordance with GMP, ISO standards and safety regulations. - Participation in the validation of manufacturing processes of pasty forms. - Control of anomalies and proposal of corrective actions - Daily Activity: technicians aid in various manufacturing tasks that allowed me to acquire a good knowledge of various manufacturing processes drugs. - Ensure implementation of production programs and procedures in accordance with GMP, ISO standards and safety regulations. - Participation in the validation of manufacturing processes of pasty forms. - Control of anomalies and proposal of corrective actions

    • Resident Pharmacist
      • Mar 2008 - Sep 2008

      Pharmaceutical hospital management Pharmaceutical hospital management

Education

  • University of Monastir, Faculty of Pharmacy, Monastir
    Specialist Diploma in Industrial and Hospital Pharmacy, Pharmaceutical Sciences
  • IPIL – University of Lyon Claude-Bernard
    Certificate of Specialized Training in IBMP (Industrial and Biomedical Pharmacy)
  • IPIL - University of Lyon Claude-Bernard
    University Diploma: Management of Industrial Systems
  • University of Monastir, Faculty of Pharmacy, Monastir
    Master M2 « Drug development», Pharmaceutics and Drug Design
  • University of Monastir, Faculty of Pharmacy, Monastir
    National Diploma of Pharmacy Studies

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