We are committed to produce our products as per international ISO/GMP standards.
Quality is the most important aspect at AllChem Asia. We always keep an eye on process performance through product conformity, corrective actions, follow up actions, and innovative GMP practices to achieve continual progress in total quality of our products and services.
It is a manufacturing facility for preparing raw materials for the manufacture of substances. Here it is being prepared for production.
We assure our customers of high quality standard backed by technical support wherever necessary. We have well equipped quality assurance department with dedicated personnel’s to check and maintain stringent product specifications matching – GMP International standards.
Our Quality Program includes:
Strict process control through in-process checks.
Stability studies.
Pre-shipment inspection and quality assurance are the major factors to deliver the product at its best.
Testing and inspection is uncompromising at AllChem Asia to ensure the quality of our products.
It is a microbiological industrial plant in which preparations based on bacteria, microorganisms and fungi are produced.
This is a premise of high-thermal production. Here, medicinal substances are produced that require a high temperature regime during production.
Technology our quality control
Quality control testing of raw materials is needed from early stage product development through to commercial batch release. The quality of raw materials can vary considerably from supplier to supplier, and even batch to batch, and so controlling the quality of the input material is key to the success of the product.
When you outsource quality control testing, you will need to select a partner with a strong history of delivering to a consistently high standard, allowing you to focus on your core business agenda.
QC testing of pharmaceutical raw materials to international pharmacopoeia specifications has become a specialty of AllChem Asia. With our knowledge of analytical chemistry and our vast range of instrumental techniques, we can undertake the vast majority of the chemical tests listed within the international pharmacopoeias.
In addition to routine QC batch release, as experienced analytical chemists, we are used to trouble shooting quality control issues and can assist you with developing a detailed specification for the material. Method development and validation services compliment pharmacopoeial testing services should specialist QC methods be required.
With our global network of GMP compliant analytical laboratories, our highly skilled scientists routinely conduct QC testing of raw materials, excipients, in-process samples and finished product batches. We tailor our QC programs to your requirements and through our wide range of GMP qualified analytical instrumentation we can provide services for the most basic of tests through to more specialized techniques, and so obtain the data you need, at the right time, to make critical quality control decisions about your product.
This is a room for the production of oil-based substances and requiring a multi-stage sterilization system.