Contact Information
Registered Office/ Head Office:
Ashford Laboratories Pvt. Ltd.,
31/36, 5th Floor, Dheeraj Heritage,
S. V. Road, Santacruz (West),
Mumbai (Bombay) - 400 054. India.
Tele- fax: + 91 22 6675 8866
Email:info@ashfordlab.com

Japan Office:
Ashford Laboratories,
4-11-24-1402 Fukae Kitamachi,
Higashi Nada Ku, Kobe 658-0013,
Japan.
Tele- fax: +81 0784 122579
Email:japan@ashfordlab.com
Our legacy of quality and environmental health & safety
A number of Operational Excellence (OE) initiatives have been developed and executed to embed a process improvement culture within our manufacturing facilities, with a focus on reducing variability and eliminating waste. Problem solving throughout the organisation is approached in a collaborative and mature manner by focusing on the needs of the customer, empowering employees, and optimising existing activities in our manufacturing, scale-up and development processes. A systematic training programme over the past five years has meant trained problem solvers (black belts,green belts and yellow belts) can anticipate, overcome and improve workflow challenges.

Our Legacy of Quality
Ashford has a proud history of quality with multiple regulatory authorities. There is a culture of ‘Building Quality’ into all we do at Ashford and this message is continually reinforced at all levels in the organisation. We have an excellent compliance record with regulatory agencies including the FDA where, for example, our plant has enjoyed zero non compliance in its last three successive inspections.

Quality & Complaince
To manufacture products that are consumed by patients across the world requires stringent standards and consistent quality assurance.

We believe it's a challenge to be a manufacturer of finished pharmaceutical formulations and herbal formulations that will be truly world class. In our quest for perfection, we have left no stone unturned right from the selection of the finest raw material, using state-of-the-art technology and processes to bringing out the finished formulations. Helping us produce the finest quality pharmaceutical products.

We take our role as a global manufacturer of finished pharmaceutical formulations and herbal formulations very seriously and surpass any standards set by worldwide regulatory authorities. All our products are manufactured as per the regulations and guidelines of the World Health Organization's Good Manufacturing Practice (WHO GMP). We implement this through our global quality management system that is based on planning, implementation and control with independent controls that guarantee safety and reliability ensuring that only the finest quality pharmaceutical products roll out of our facility.

Our credentials include an ISO 9001: 2008 certification issued by Norwegian Accreditation USA. This establishes firmly that we are manufacturer of finished pharmaceutical formulations and herbal formulations of high quality.

The above initiatives are backed by an independent unit that analyses, evaluates and reports the status of quality control and quality assurance. They give accurate and accountable results that help us produce the finest quality pharmaceutical products always.

Our commitment to quality and regulatory affairs is one of full compliance, be they local, national or international standards or norms and regulations. A dedicated Quality Control Department and a strict Quality Assurance Policy guarantees consistent quality of all our processes and products.

It is due to our quality and delivery of innovative drugs and discoveries by adhering to ISO/GMP norms and discharging our duties respecting the laws of the land, that we have been attracting clients from different parts of the world.

Following aspects are continuously monitored to ensure consistent level of quality
Suppliers : Conducting thorough Audits/Evaluation of raw material suppliers for consistency, quality and reliability.

Raw Materials : A unique batch number identifies every raw material. It is kept under quarantine and later sampled and tested for conformity to the required specifications. Only when the Q.C. dept. approves and releases the raw materials they are issued for appropriate usage.

In-Process Controls : Every manufacturing process is checked to verify correct course and completion of the process in conformity with the standard operating (SOP's) procedures. Instructions are followed strictly and no deviations are allowed to ensure best quality of the final product.

Finished Product : All finished products must display purity and quality, for intended use in compliance with the specifications of Genesis, Clients and Pharmacopoeias.

Packaging : Packaging is carried out in such a way that cross contamination or errors have 'no room' to be committed. All products are packed as per international standards, to ensure product safety.

Labeling : Labels are stuck at appropriate positions, as required by the clients/Authorities. Outdated labels are destroyed on a periodical basis.

Shipment : All Shipments / Dispatches are checked and recorded.

Delivery : Transportation and Delivery is carried out with care and punctuality.

ISO 9001 Certification : All our processes are conducted as per the guidelines provided in ISO specifications.

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