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Share Formula Record Feature

Discover the Share Formula Record feature, a tool designed to enhance collaboration and streamline your workflow. This feature allows you to easily share your formula records with team members or clients, ensuring everyone stays on the same page.

Key Features

Easy sharing options for quick collaboration
Secure access controls to protect your data
User-friendly interface for effortless navigation
Real-time updates to keep everyone informed
Compatibility with various platforms for seamless integration

Potential Use Cases and Benefits

Collaborate with team members on project formulas
Share records with clients for transparency and trust
Facilitate training sessions by providing access to formula records
Collect feedback efficiently by sharing specific records
Improve productivity by reducing time spent on sharing information

The Share Formula Record feature addresses common challenges in communication and collaboration. It simplifies the process of sharing crucial information, freeing you from cumbersome methods that often lead to confusion or lost data. By implementing this feature, you can ensure clarity and efficiency in your work environment, ultimately enhancing productivity and fostering stronger team dynamics.

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Master formula record (MFR) is a master document for any pharmaceutical product. A MFR should have following parts: Product Details: First on the first page following details about the product are added. Name, logo and address of the manufacturing company. Dosage form name. Brand name. Generic name. Product code.
MASTER FORMULA — A document or set of documents specifying the raw materials with their quantities and the packaging materials, together with a detailed description of the procedures and precautions required to produce a specified quantity of a finished product.
MASTER FORMULA RECORD Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units.
In the compounding pharmacy this document is called the Master Formulation Record (MFR). It is comparable to a recipe in cooking. For a given preparation, the MFR is prepared before the preparation is compounded. The CR is used during the preparation to guide and record the actual process.
3.2 Batch Formula (name, dosage form) A batch formula should be provided that includes a list of all components of the dosage form to be used in the manufacturing process, their amounts on a per-batch basis, including overages, and a reference to their quality standards.
Batch manufacturing record is a written document from the batch that is prepared during the pharmaceutical manufacturing process. It contains actual data of the batch manufacturing and whole manufacturing process step by step. There are several stages of the pharmaceutical product manufacturing process.
Batch manufacturing record is a written document of the batch, prepared during pharmaceutical manufacturing process. It contains actual data and step-by-step process for manufacturing each batch. Batch manufacturing record is like a proof that batches were properly made and checked by quality control personnel.
Ensure the 'Weight Verification' of all 'Dispensed Materials' is completed and signed prior to manufacturing. Ensure the 'Environmental Condition Log' is written as per Instruction given in BMR. Check the Line clearance is verified by QA. Ensure the Sieve/Screen is used as per mention in the batch record.

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