REVIEW

How to Review Your Product Range Once a Year

An annual review catches the things that decay quietly: expired certificates, stale artwork, marginal SKUs and documentation nobody updated. It takes a day once a year and prevents most of the problems that otherwise surface through a buyer audit or a complaint.

CadenceOnce a year
CatchesQuiet decay
DecideKeep or discontinue
RefreshLicences and artwork

What Decays Without Anyone Noticing

This guide is for supplement, Ayurvedic and herbal brand owners in India.

Several things in a product range lose currency silently. Licences and certifications reach their renewal dates. Artwork files drift out of line with the formulation after a change. Certificates of analysis accumulate unread. A SKU stops selling without being discontinued. Claims written two years ago sit on listings nobody has reviewed.

None of these announces itself. They surface when a buyer asks for documentation, a marketplace removes a listing, or a complaint arrives about a product whose records are incomplete.

An annual review catches all of them, and it is a day’s work rather than a project.

Schedule it: Put it in the calendar as a recurring commitment. A review that depends on remembering does not happen.

What to Review Per SKU

Work through every product.

  1. Licence and certification validity, yours and your manufacturer’s, with renewal dates noted.
  2. That the manufacturer’s licence scope still covers the product.
  3. That the specification on file matches what is actually being produced.
  4. That artwork on file matches both the specification and what is printed.
  5. That the artwork compliance review record exists and reflects the current version.
  6. That stability data still covers the current formulation and pack.
  7. That certificates of analysis are complete for every batch received, and were checked.
  8. The batch log, for any drift in key values.
  9. Complaint history by cause, and whether anything recurring was addressed.
  10. Reorder rate and contribution per order.
  11. Whether the physical reference sample needs refreshing.
  12. Whether all listings and marketing match the current approved claim set.

Range-Level Decisions

Beyond individual SKUs.

Question What to Look At
Which SKUs to keep Reorder rate and contribution, not revenue
Which to discontinue Marginal SKUs consuming minimums and attention
Which to reformulate Recurring complaint causes you have not addressed
Where to share components Containers and closures used by only one SKU
Where pack sizes conflict Durations that produce awkward reorder rhythms
Whether the claim set is current Changes in your products or in guidance
Whether procedures match practice Written processes that have drifted from reality
Supplier performance Documentation quality, consistency and responsiveness

The discontinue decision is the one most often avoided. A marginal SKU consumes packaging minimums, stability work, listing maintenance and attention, which makes it more expensive than its margin suggests.

Housekeeping Worth Doing

Small tasks that prevent larger problems.

Replace Expired Documents

Update licence and certificate copies in each product file and note the new validity dates.

Run the Traceability Test

Pick one batch and reconstruct its full history. Close whatever gaps appear.

Refresh Reference Samples

Retained samples age. Replace them from a current batch and note which batch.

Archive Discontinued Products

Keep files for products still within shelf life in the market, archived rather than deleted.

Also re-read your own listings and website as a buyer would. Claim drift is easiest to spot after a year away from the copy.

Review Checklist

Work through once a year.

  1. Schedule the review as a recurring commitment.
  2. Check licence and certification validity for every product.
  3. Confirm manufacturer licence scope still covers each product.
  4. Reconcile specification, artwork and actual production.
  5. Confirm the artwork compliance review record is current.
  6. Confirm stability data covers the current formulation and pack.
  7. Check certificates of analysis are complete and were reviewed.
  8. Review the batch log for drift.
  9. Review complaint history by cause and act on recurring items.
  10. Review reorder rate and contribution per SKU.
  11. Decide which SKUs to keep, reformulate or discontinue.
  12. Identify component sharing opportunities.
  13. Re-read all listings and marketing against the current claim set.
  14. Run the traceability test on one batch.
  15. Refresh retained reference samples.
  16. Archive files for discontinued products.
  17. Record what you decided, so next year has a baseline.

Need Current Documentation Across Your Range?

Share your product list and our team will provide up-to-date licences, specifications and batch documentation.

Get in Touch →

Frequently Asked Questions

What decays without anyone noticing?

Licence and certification validity, artwork drifting out of line with the formulation, unread certificates of analysis, SKUs that stopped selling without being discontinued, and claims on listings nobody has reviewed in years.

How long does an annual review take?

Around a day for a modest range, provided product files exist. It is housekeeping rather than a project, and it prevents most of the problems that otherwise surface through a buyer audit or a complaint.

What should drive the keep-or-discontinue decision?

Reorder rate and contribution per order rather than revenue, and counting the hidden cost: packaging minimums, stability work, listing maintenance and attention. A marginal SKU is more expensive than its margin suggests.

What housekeeping is worth doing each year?

Replacing expired licence and certificate copies, running the traceability test on one batch, refreshing retained reference samples, archiving files for discontinued products, and re-reading your own listings as a buyer would.

Should files for discontinued products be deleted?

No, archived. Units may remain within shelf life in the market, and a complaint about a discontinued product still requires the specification, certificates and batch records to answer properly.

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