YOUR TRUSTED PARTNER IN PHARMACEUTICAL COMPLIANCE

Expert Guidance for Quality, Regulatory and Operational Success

TRANSFORM YOUR QUALITY

FROM REACTIVE TO READY

LabQ International Pvt Ltd has been providing services in the field of GxP Sciences for the last 15 years in the UK, EU, MENA and the US.

Navigate regulatory challenges with our end-to-end compliance solutions. From identifying risks with Gap Assessments to building team skills with GxP Training, we cover every angle. We are your partners in building robust quality systems that are always ready for inspection.

GXP SERVICE PORTFOLIO

Specialised in audits and inspections from a wide range of regulatory agencies, not limited to: US FDA, EMA, MHRA, HPRA, TGA, SFDA, CFDA, ANVISA and more

From ICH GCP E6(R3) to PIC/s, CSV Guidance, CQV, and more

Preparation of your organisation for inspections on a short and long-term basis

Gap assessments to US FDA, EMA, MHRA, HPRA, TGA, SFDA, CFDA, ANVISA and other regulators

Audits &

Inspections

GxP Training

Inspection

Readiness

Gap Assessments

GLOBAL REACH

UK | USA | EU | MENA | Asia

5-STARs

15+ years in service

50+ satisfied clients

A-TEAM

20+ consultants with over 500 years' combined experience

GxP Services

ONE-STOP SHOP CONSULTANCY

We believe in a tailored solution for individual client need rather than using a holistic singular approach since each client has their own set of conditions and the environment in which the GxP services need to be tailored towards

Audits and Inspections

Let our team support you in conducting independent audits for various entities such as CMOs, CDMOs, CROs, GLP and Central Labs, AI service providers, investigational sites, and other vendors.

GxP Gap Assessments

We provide gap assessments to various standards and regulations including but not limited to US FDA, EMA, PIC/s, MHRA (UK), ICH and other as relevant. Our process is simple and tailored to suit your organisational objectives.

We also help with remediation and mitigation plans post assessment and also in case of inspection findings.

GxP Training

We provide GxP training remotely, onsite, and workshop settings on the following, but not limited to:

ICH GCP Guidelines (incld updates to E6)
PIC/s Guidelines
EMA Statutory Instruments and Guidance Documents
US FDA Guidance Documents and Code of Federal Regulations (CFR)
Risk-based Audit and Vendor Management
Quality Risk Assessment (ICH Q9)
Inspection Readiness
Mock Inspections and Preparation

Aim for Quality by Design not Quality by Accident

Dr. Shahid A Syed

Sr Consultant

Don't prepare for inspections - prepare for Quality. Inspection Readiness should be a "state" you live in rather than a "rushed event".

Saqib Choudhary (PhD, MD)