Quality Aspects

We at Chromato Scienitific, we have a full Quality Management System to control the Quality from concept to Commercialization.

• Quality planning: At Chromato Scientific, quality is part of each and every step. Planning focuses on all areas of operation comprising procurement of the raw materials, to synthesis, then Storage and precise delivery as per customer's requirements.
• Quality assurance: Chromato Scientific's Quality Assurance Department, constantly monitors and appraises the service as per SOP’s to ensure requirements for Quality are being satisfied.
• Quality control: Chromato Scientific embraces, a full-fledged Quality Control Laboratory, which follows and integrates up-to-date, contemporary, and high-tech testing equipment, in order to perform the stringent quality analytical tests like HPLC/GC, Mass Spectroscopy, IR Spectroscopy, Thermal Gravimetric Analysis (TGA).
• Quality improvement: Chromato Scientific is dedicated and committed to delivering value and satisfaction by improving and maintaining the Quality Management System through meeting specific needs, training to an individual, CAPA, Clean Work Environment.
• Document Control: At Chromato Scientific, Document and Data are maintained to control all documents that form part of its management system, internally generated or from external sources, including SOP’s with master and Controlled Copy, Test and Calibration Records, Soft copy of Data on Server.
• Audit Management: Chromato Scientific conducts periodic self-assessments through a voluntary self-audit of its operations, in order to remain internationally competitive, and maintaining an effective Quality Management System.
• CAPA Management: At Chromato Scientific, we Follow CAPA management for any Discrepancies and Audit Findings. It assures the tracking and trending of issues requiring mid-term and long-term corrective actions.
• Training Control: Chromato Scientific has an effective training Execution from Induction to SOP and Practical training to Presentations, so that the entrant is fully aware of well-being at Chromato Scientific.

At Chromato Scientific, we Qualify the Synthesized compounds for Identification / structure elucidation and Qualification by HNMR and 13C-NMR, MASS, IR Spectroscopy, CHNS and Purity by HPLC/GC/Chemical Analysis. Purity/Potency is defined by Mass Balance Method using Chromatographic purity and TGA Data, For Volatile Compounds Ash Content is performed.

After Qualification, product is sent into Global Warehouse. Inventory Team Checks the product for Quality, from Description to all Characterized Data and approves the qualification Report with interpretation of all Data.

Once the Material is Qualified and Approved, it is taken into Approved Area and made available for Dispatching.

Before Dispatch, the material is again Reviewed and Checked by Dispatch QA. Once the Dispatch QA approves the Quality and Documents as per Specification, it is ready to Dispatch.