Skip to content
Intra Mesk Pharma — انترا مسك فارما

Warehousing & Cold Chain

Controlled Storage for Product Quality and Integrity

Appropriate storage is an essential part of maintaining product quality and integrity across the healthcare supply chain.

Intra Mesk Pharma manages products according to their applicable storage, handling and environmental requirements, with particular attention to temperature-sensitive products where controlled conditions are required.

The Central Idea

Storage Is Part of Product Management

A product does not stop requiring appropriate control when it reaches a warehouse.

Its storage environment, handling requirements, status and relevant information remain important throughout the period in which it is held.

Our approach is therefore based on understanding the requirements applicable to the product and maintaining appropriate conditions within the stages under our responsibility.

This includes receiving, storage, stock handling, order preparation and dispatch, as applicable to the product and operating process.

Product status

Where a product stands — incoming, held, released, stored, allocated or dispatched — each status with its own controls.

Environmental control

The conditions a product is kept in: ambient, temperature-controlled or cold chain — understood, monitored, recorded and answered to.

Product Status

Product Status Matters

Products entering storage are not treated as undifferentiated inventory.

Relevant product and shipment information, receiving status and applicable storage requirements help determine how products are handled within the warehouse environment.

This supports a clearer relationship between product identity, condition, storage location and subsequent distribution activity.

  1. Purpose

    Bring products into the warehouse through one controlled receipt point.

    High-level control

    Products enter against documentation, before any other status applies.

    What happens next

    Products move into quarantine status — they are not yet available.

  2. Purpose

    Hold products in a segregated status while verification is pending.

    High-level control

    Held stock is physically and systematically separated from available stock.

    What happens next

    Verification — the point where the next status is decided.

  3. Purpose

    Check the product and its documentation before release.

    High-level control

    Ready products proceed to release; anything not ready is held under control.

    What happens next

    A status decision: release — or hold / control.

  4. Ready → Release
    Not ready → Hold / Control
  5. Purpose

    Make verified products available for storage and order fulfilment.

    High-level control

    Only released products enter the storage that serves customer orders.

    What happens next

    Storage — placed according to the applicable conditions.

  6. Purpose

    Hold released products under the conditions applicable to them.

    High-level control

    Where products are stored reflects what they are and what they require.

    What happens next

    Picking, when an order calls for the product.

  7. Purpose

    Select and assemble products against a specific order.

    High-level control

    Picked stock is checked against the order it is allocated to.

    What happens next

    Dispatch — checked shipments are released to distribution.

  8. Purpose

    Release checked shipments into the distribution flow.

    High-level control

    The warehouse journey ends where distribution control begins.

    What happens next

    Continue on the Distribution & Logistics page.

Hold / Control

Products that are not ready stay under control until a status decision is possible.

Return

Returned products follow a defined handling pathway of their own.

Reject / Expire

Segregated holding pending documented disposition.

A public explanation of how product status works — not an internal SOP, and not a disclosure of disposition criteria.

Controlled Environments

Environmental Conditions Follow Product Requirements

Storage conditions must reflect the characteristics and requirements of the product.

Some healthcare products require controlled temperatures, protection from environmental conditions, or specific handling precautions.

Temperature-sensitive products require particular attention to maintaining the applicable conditions throughout relevant storage and movement stages.

+15 … +25 °C

Ambient

For products requiring no temperature control.

+8 … +15 °C

Temperature-Controlled

Cool conditions for products that require them.

+2 … +8 °C

Cold Chain

For applicable cold-chain products.

Where a product requires a controlled cold-chain range such as 2–8°C, that requirement is treated as a product-specific condition rather than a generic warehouse setting.

Cold Chain

Cold Chain Requires Continuity of Control

Cold-chain management is not limited to maintaining a temperature range inside a storage area.

  1. Import
  2. Receive
  3. Quarantine
  4. Controlled Storage2–8°C
  5. Pick
  6. Transport
  7. Delivery

Product requirements must be considered during receiving, temporary handling, storage, preparation and movement through the relevant supply stages.

Maintaining the applicable conditions across these stages supports product integrity and reduces the risk of inappropriate exposure.

The exact temperature requirements depend on the product and its applicable conditions.

Traceability

Storage and Traceability Work Together

Good storage control also depends on knowing what is being stored, where it is located and how it moves through the distribution process.

Relevant records and product information help connect receiving, storage, stock movement and distribution.

Traceability supports appropriate review when a discrepancy, quality concern or product-related question requires follow-up.

  1. 01

    Understand

    Know the applicable product and storage requirements — including how storage areas behave.

  2. 02

    Monitor

    Observe relevant environmental conditions where products are stored and handled.

  3. 03

    Record

    Maintain relevant records and data so conditions remain reviewable.

  4. 04

    Respond

    Apply appropriate actions when conditions require attention — so continuity of control is protected.

  5. The control stack operates as one loop — each layer feeds the next. Technical thresholds and internal protocols are not published here.

Status Under Question

When product status changes

A released status is not permanent. Concerns, returns and other events can bring a product's status into question — and the response follows the same discipline.

  1. Released

    Product available as normal stock.

  2. Concern / Return

    A concern or return brings the status into question.

  3. Segregate / Control

    The product is separated from available stock.

  4. Assess

    The situation is reviewed and understood.

  5. Disposition

    A documented decision completes the change.

A status change is handled with the same discipline as any other warehouse control — segregation, assessment and a documented disposition. Internal decision authorities are not described here.

Operating Facilities

Anchored in Sana'a and Aden

Two principal operating facilities support pharmaceutical warehousing and distribution activities.

Sana'aAden

Sana'a

Fiftieth Street, near Y Telecom, Republic of Yemen

Primary Operating Facility

Aden

Al-Mansoura, Ninetieth Street

Primary Operating Facility

The Warehouse Flow

From Receiving to Dispatch

Products move through a defined warehouse sequence under the conditions applicable to them.

  1. 01Receive
  2. 02Verify
  3. 03Store
  4. 04Prepare
  5. 05Dispatch
  1. 01

    Products enter the warehouse through a defined receiving process.

  2. 02

    Product identity, shipment information and relevant condition are reviewed.

  3. 03

    Products are maintained under applicable storage conditions.

  4. 04

    Products are selected and prepared for distribution according to the relevant process.

  5. 05

    Products are released for movement through the applicable distribution process.

People & Responsibility

Storage Depends on Disciplined Operations

Storage conditions are supported by defined responsibilities, consistent handling practices and appropriate attention to product status and environmental requirements.

The purpose is not simply to maintain inventory. It is to maintain products in an appropriate condition until the next controlled stage of their movement.

Portfolio Development

Storage Capability Follows Product Scope

As the range of healthcare products handled by Intra Mesk Pharma develops, storage requirements are considered according to the characteristics of each product category and supply arrangement.

The company evaluates product-specific storage and handling requirements as part of its operating approach.

Explore Distribution & Logistics

See how controlled storage connects to organized distribution across the healthcare supply chain.