About Aan Lifescience
We are a firm of Technological advancement set up in line with WHo-GMP, PICS-GMP norms to provide best in class pharma care

AAN Lifescience Private Limited has been promoted by experienced professionals in the same line of business. The promoters are operating Aan Pharma Private Limited has been involved in manufacturing of Tablets, Capsule, Ointments and Liquid orals since 1994. AAN Lifescience is a step forward in technological advanced set coming up with the state of the art manufacturing facility at Ghodasar Village in Mehmedabad taluka and Kheda District of Gujarat

Company’s upcoming facility will comprise of Beta lactam Tablets, Capsules and Dry powder. The facility will be in accordance to WHO-GMP, PICS-GMP norms and various registrations will be taken forward.

The manufacturing plant will be state of the art unit having latest technology with minimal human intervention equipped with latest QA, QC and F&D departments. The plant functional on single shift installed capacity of 25 lacs Tablet, 5 lacs Capsules and 40,000 Dry powder bottles.

The initial focus of the company shall be operating the plant on contract manufacturing with and endeavor in the export market.

Vision Of The Aan Lifescience

  • Latest Technology
  • Pro-active Team empowered with relevant Know-how
  • Best of the Services

Technology

  • AAN Lifescience Private Limited will be equipped with top of the line equipments from the most reliable names in the sector with latest state-of-the-art technology in as well as infrastructure complied with WHO-GMP, PICS-GMP standards.
  • To achieve best of the results, the company has acquired best of the technology and machines in its entire product range.
Production
  • The production supervisor rechecks the weights of dispensed material in production department
  • Manufacturing process is done strictly as per procedure given in MFR. GMP is strictly followed
  • The BMR moves along with the product from section to section and all relevant entries are recorded as the process progresses
  • The first three batches of any product are manufactured jointly by R&D and Production Department and are evaluated by the Quality Assurance Department
IN-PROCESS QUALITY EVALUATION
  • Q.A. personnel will perform in-process checks to ensure that activities are carried out as per SOP and products are manufactured as per the prescribed standards
  • Q.C. Department tests the composite samples of granules / tablets before they are taken for further processing
  • The batches are analyzed as per the documented specifications
  • The results of complete analysis are entered in the protocols and the Certificate of Analysis is prepared. One copy of COA is sent to production section for attachment in BMR
  • RELEASED labels are affixed on the bulk containers and then the batch is sent to the next stage of processing along with BMR
  • All materials of previous products are removed from the area before starting next product and line clearance is obtained from Q.A. Department
  • Product changeover on the machine & its clearing is done as per SOP
  • Q.A. Department gives line clearance report before starting of filling/compression and packing operation. For tablets to be coated, they are coated only after Q.C. release of core tablets
  • The coated tablets are again analyzed by Q.C. Department. After release of coated tablets, they are transferred to blister/packing section
  • I.P.Q.C. chemist carries out weight variation, leak test and all other in process checks required to be carried out during filling/packing operations
  • Production chemist checks the process control parameters
  • Q.C. personnel draw sample from finished packs for testing and to preserve the required no. of packs for Control Sample
  • Q.A. ensures that BMRs are complete in all respects. The release for sale is given by the Q.A. Manager only after complete analyses of the product as per the Standard specifications and meeting of other parameters including the documentation
Quality Assurance
Mission’s Quality Policy has a broad base, with stringent specifications to ensure all Quality parameters. Our strong belief in quality is not only restricted to conformance of written specifications but also to build all employees into a team that believes in quality in the product at every stage of manufacture. The system is designed in such a way that all aspects of G.M.P. and G.L.P. are followed by means of using :
  • Best available resources
  • Vendor Rating and Approval
  • Good Product Design
  • Validated Processes
  • Well Trained Personnel
  • Stringent Quality Control
  • Effective Quality Assurance
IMPLEMENTATION OF QUALITY POLICY
To achieve quality objective a strong Quality Assurance System has been formulated incorporating Good Manufacturing Practices and Good Laboratory Practices.
  • Perform Vendor Evaluation
  • Oversee all Quality Control Norms
  • Perform Process Evaluation
  • Examine current methods of analysis to confirm suitability
  • Interact with R&D to evaluate suitable specifications for Raw Materials, Packing Materials and Finished Products.
  • Monitor ongoing Stability Studies
  • Review MFR Periodically
  • Ensure GMP and GLP at all stages
  • Investigates market complaints and product recalls
  • Preserve control samples, working standards etc.
  • Assist in self-quality Audit
  • Periodically conduct Self-Inspection and Audit
  • Co-ordinate and provide appropriate training to all Personnel
  • Review all Statutory compliances
  • Master Formula Record of each Product
  • Master Formula Record of each Product
  • Batch Manufacturing Record
  • Batch Packing Record
  • Batch Dockets
  • I.P.Q.C./Process Control Records
  • Standard Operating Procedures
  • Standard Cleaning Procedures
  • Periodical review of all the above documents
  • Updating as per the Standard Norms
Quality Control is that part of Quality Assurance System which is concerned with sampling, specifications and testing within the organization, documentation and release procedures which ensure that necessary and relevant tests are actually carried out and that materials are not released for use nor products released for sale and supply until their quality has been confirmed to satisfactory. Quality Control Personnel perform the following functions :
  • Inspect the consignment, perform sampling and analysis at various stages of manufacturing operations
  • Assign reference number for release of Raw materials, Packing materials and Finished products
  • Assign reanalysis data etc. for various materials & advise store on their storage conditions
  • Preserve control samples, working standards etc
  • Monitor ongoing stability studies
  • Verify dispensing of the Materials as per BMR in the dispensing area
  • Review records, control samples and ensure disposal of old records, samples etc
  • Preserve reports, records and documents
  • Assist in calibration of in-process control instruments, laboratory instruments
  • Validation of equipments, processors etc
  • Ensure proper disposal of rejected material/products
  • Monitor line clearance, in-process control review and approve BMRs
  • Monitor line clearance, in-process control review and approve BMRs
  • Release finished products for sale
While adequate facilities are provided in-house for all testing and evaluation, for some of the tests where it is not commercially viable as yet, outside assistance is obtained.
Public Laboratories are identified and chosen by a systematic evaluation and approval. Such contract Laboratories are periodically inspected based on the frequency and feasibility in a progressive manner. Increased Self-reliance will be achieved.
The Unit

Aan Lifescience Private Limited has acquired land of approx. 6500 sq. yards in vicinity of developed industrial locality of Ghodasar village, Mehmdabad taluka. the promoters has also acquired the adjacent plot of the similar area for the future expansion. The unit is planned with built up area of appx 60,000 sq fts to be developed at a cost of appx Rs.10 cr. The Planning and designing of the building is done by the leading consultants specialized in the sector with very high experience.

Promoters

Mr. Ashwin N. Shah

Mr. Ashwin Shah aged 66 is a 1st generation entrepreneur involved in the Pharmaceutical business since more than 4 decades, Mr. Ashwin Shah started his career from a small distribution ship, moved forward and became partner in Jaywin Remedies in 1984. In the year 1994, Mr. Ashwin Shah incorporated Aan Pharma Private Limited with an objective on entering in pharmaceutical mfg. business. In the initial years the products marketed were manufactured on loan and license from WHO-GMP registered units. Later on he expanded a manufacturing setup which has been timely expanded with the development of the market.

Mr. Maulik A. Shah

Mr. Maulik Shah aged 35 years is 2nd generation entrepreneur and is a qualified B.Pharm with Masters in Business Administration (MBA). Maulik joined Aan Pharma Private Limited post completion of his post graduation and has been instrumental in the growth of the company with expansion of Volume and Value creation. He has a dynamic quality of relation building and at present he is Executive Committee member of India’s biggest Pharma Mfg. Association – IDMA. He is also the partner in Construction site named VIAAN BUILDCON.