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How to grow your Pharma Business?

  Growing a pharma business requires a strategic approach considering the specific context of your company and the pharmaceutical industry as a whole. Here are some general pointers to get you started: Market and Customer: Identify your target customer: Deeply understand the specific needs and challenges of your target audience, whether it's doctors, patients, hospitals, or other healthcare providers. This helps tailor your products, services, and marketing efforts. Focus on unmet needs: Look for gaps in the market where existing solutions are inadequate or unavailable. Addressing unmet needs can give you a competitive edge and drive innovation. Track market trends: Stay updated on regulatory changes, technological advancements, and emerging diseases to adapt your approach and anticipate future opportunities. Products and Services: Invest in R&D: Develop innovative products or differentiate existing ones through unique formulations, delivery methods, or combinations. Remember
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Batch Processing Records

Batch Processing Records:

1. There shall be Batch Processing Record for each product. It shall be based on the relevant parts of the currently approved Master Formula. The method of preparation of such records included in the Master Formula shall be designed to avoid transcription errors.
2. Before any processing begins, check shall be performed and recorded to ensure that the equipment and work station are clear of previous products, documents or materials not required for the planned process are removed and the equipment is clean and suitable for use.
3. During processing, the following information shall be recorded at the time each action is taken and the record shall be dated and signed by the person responsible for the processing operations: -
  • The name of the product,
  • The number of the batch being manufactured,
  • Dates and time of commencement, of significant intermediate stages and of completion of production, 
  • Initials of the operator of different significant steps of production and where appropriate, of the person who checked each of these operations, 
  • The batch number and/or analytical control number as well as the quantities of each starting material actually weighed, 
  • Any relevant processing operation or event and major equipment used,
  • A record of the in-process controls and the initials of the person(s) carrying them out, and the results obtained,
  • The amount of product obtained after different and critical stages of manufacture (yield),
  • Comments or explanations for significant deviations from the expected yield limits shall be given,
  • Notes on special problems including details, with signed authorization, for any deviation from the Master Formula,
  • Addition of any recovered or reprocessed material with reference to recovery or reprocessing stages.
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