Chemo Test Way

Our adherence to global standards and and data integrity

The Chemo Test Way: Standardized & Compliant

At Chemo Test Laboratory, we foster a positive, results-driven work environment that offers continuous learning opportunities at every stage. Our workplace culture is built on collaboration, professional growth, and innovation, ensuring that every team member can learn, evolve, and thrive. We take pride in our supportive and inclusive work atmosphere, where colleagues uplift each other, leaders inspire and motivate, and a secure work environment allows individuals to excel with confidence.

We take pride in our supportive and inclusive work atmosphere, where colleagues uplift each other, leaders inspire and motivate, and a secure work environment allows individuals to excel with confidence.

01

Upgrade & Improve

  • Our skill & knowledge and managerial abilities
  • Quality of work

02

Follow

  • Verified & well documented procedures for analysis

03

Maintain

  • Valid records and documents
  • Quality Management System ISO 9001:2015 & ISO 17025:2017

04

Trust

  • Highest degree of confidentiality & impartiality

Our commitment to Data Integrity - The ALCOA++ approach

At Chemo Test Laboratory, data integrity is at the core of our quality commitment. We rigorously follow the ALCOA++ framework. This structured approach enables us to maintain the highest standards of reliability and regulatory compliance across every stage of testing and reporting

Robust Access Control for Secure and Compilant Operations

To maintain data integrity and ensure regulatory compliance, Chemo Test Laboratory implements a comprehensive user access management system. Each user is assigned specific roles and privileges based on their responsibilities, with strict controls over login credentials, role assignment, and password policies. This structured approach supports traceability, accountability, and adherence to 21 CFR Part 11 guidelines.

  • Role-Based Access Control
  • Defined Rights & Privileges
  • Administrator-Only Control
  • 21 CFR Part 11 Compliance
  • Password Security Protocol

Separate Logins for User Categories

Distinct login credentials are provided for each user category

Audit Trail & Compliance

21 CFR regulations compliant

Users are categorized

Administrator; QA Reviewer; Technical Reviewer; QC Reviewer; User/Analyst

Role & Privilege Management

Only Administrators have the authority to add or delete roles and privileges

Defined Rights & Privileges

Clear definitions of rights and privileges for each user group

Password Validity

Updated every 90 days for security purposes