Dispatch of Finished Goods

Dispatch of Finished Goods

Procedure

Arrange the pallets in the warehouse in an orderly manner.

Place the finished goods, product wise on the pallets in the Finished Goods store.

Arrange one product on one pallet.

Place the batch of the product wise.

After QC and QA release of the batch as per the procedure defined in SOP “Release of Finished Products”, the batch shall be dispatched as given below.

The batch should be dispatched on First First basis.

Dispatch

Fill the following columns of the invoice of the products which are being dispatched as per the consignee’s order including:

  • No.
  • Description of Goods / Name of the medicine
  • Name & Address of consignee on the invoice
  • Batch no.
  • Expiry date
  • Packing
  • of Corrugated boxes
  • Quantity in each corrugated box
  • Total Quantity
  • Rate per unit
  • Deduction under section 4
  • Assessable value per unit
  • Total assessable value

Each invoice has four copies :

Original for buyer

Duplicate for transporter

Triplicate for our accounts dept.

Fourth (extra) copy for factory record

Collect the material to be dispatched outside the warehouse and carefully check the batch no. of the products to be dispatched from the invoice to avoid the dispatch of wrong batches to the consignee and then load the products in the vehicle.

Maintain the dispatch record on the computer.

Check the computer record and invoice for tracing the distribution record in the future.

About Abha Maurya

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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