Smart, Risk-Based Validation for a Safer World

We help pharma and med-tech teams deliver safe, compliant products through lean, risk-based CQV, CSV, PV, and aseptic validation

WHY US

Why Choose Validation Solutions?

Built on EU GMP, FDA, GAMP 5 and ICH Q9 principles our approach delivers lean, defendable validation

Risk-based

We start every validation with a robust risk assessment aligned to ICH Q9 and EU GMP. This keeps your project lean—no over-validation

Lean

We streamline validation to remove waste and accelerate delivery while maintaining compliance and patient safety.

Tailored

Every facility, system, and process is different. Our validation strategies are tailored to your site, equipment, products, and regulatory needs.

Trusted

Hands-on industry experience across aseptic, biotech, and med-tech. Our documents withstand audits, our approach builds confidence

SERVICES

Smart, Lean, and Compliant Validation Services

Smart, Lean, and Compliant Validation Services

DELIVERABLES

What can you expect from us?

Fast response and project turnaround

Regulatory-compliant documentation

Experienced validation specialists

Transparent pricing structure

Continuous support post-project & audit readiness.

TESTIMONIALS

“Validation Solutions made the entire CQV process smooth and efficient. Their team understood our needs, stayed compliant, and helped us meet deadlines without unnecessary complexity. Truly reliable partners”

“Validation Solutions made the entire CQV process smooth and efficient. Their team understood our needs, stayed compliant, and helped us meet deadlines without unnecessary complexity. Truly reliable partners”

— Sam Anderson

FAQ

Frequently Asked Questions

Still got questions? Feel free to reach out to us
What types of validation projects do you support?

We handle CQV, CSV/CSA, Process Validation, Cleaning Validation, Aseptic/Annex 1 qualification, VHP cycle development, facility qualification, and more.

How quickly can you start?

Most projects can begin within 24–72 hours, depending on scope. For urgent issues (audit findings, Annex 1 gaps, system go-lives), we prioritise immediate support.

Can you work within our internal QMS, templates, and SOPs?

Absolutely.
 We align all deliverables with your internal QMS, templates, and site procedures so your documents integrate seamlessly.

What industries do you work with?

Pharmaceutical, biotech, medical device, ATMP, compounding, and aseptic manufacturing environments.

Do you offer ongoing support after project completion?

Yes. We remain available for future batches, periodic reviews, requalification, change controls, audit readiness, and any follow-up required.

What types of validation projects do you support?

We handle CQV, CSV/CSA, Process Validation, Cleaning Validation, Aseptic/Annex 1 qualification, VHP cycle development, facility qualification, and more.

How quickly can you start?

Most projects can begin within 24–72 hours, depending on scope. For urgent issues (audit findings, Annex 1 gaps, system go-lives), we prioritise immediate support.

Can you work within our internal QMS, templates, and SOPs?

Absolutely.
 We align all deliverables with your internal QMS, templates, and site procedures so your documents integrate seamlessly.

What industries do you work with?

Pharmaceutical, biotech, medical device, ATMP, compounding, and aseptic manufacturing environments.

Do you offer ongoing support after project completion?

Yes. We remain available for future batches, periodic reviews, requalification, change controls, audit readiness, and any follow-up required.

What types of validation projects do you support?

We handle CQV, CSV/CSA, Process Validation, Cleaning Validation, Aseptic/Annex 1 qualification, VHP cycle development, facility qualification, and more.

How quickly can you start?

Most projects can begin within 24–72 hours, depending on scope. For urgent issues (audit findings, Annex 1 gaps, system go-lives), we prioritise immediate support.

Can you work within our internal QMS, templates, and SOPs?

Absolutely.
 We align all deliverables with your internal QMS, templates, and site procedures so your documents integrate seamlessly.

What industries do you work with?

Pharmaceutical, biotech, medical device, ATMP, compounding, and aseptic manufacturing environments.

Do you offer ongoing support after project completion?

Yes. We remain available for future batches, periodic reviews, requalification, change controls, audit readiness, and any follow-up required.

Still have questions? Reach out to us & we'll help
Still have questions? Reach out to us & we'll help

DISCOVERY CALL

Were ready when you are

Book a free discovery call & lets see if were a good fit

DISCOVERY CALL

Were ready when you are

Book a free discovery call & lets see if were a good fit

DISCOVERY CALL

Were ready when you are

Book a free discovery call & lets see if were a good fit

VALIDATION

SOLUTIONS

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Book a free 15 minute consultation call & let’s get started

VALIDATION

SOLUTIONS

Book a free 15 minute consultation call & let’s get started

VALIDATION

SOLUTIONS

Book a free 15 minute consultation call & let’s get started

SERVICES

What can you expect from us?

Fast response and project turnaround

Regulatory-compliant documentation

Experienced validation specialists

Transparent pricing structure

Continuous support post-project

SERVICES

What can you expect from us?

Fast response and project turnaround

Regulatory-compliant documentation

Experienced validation specialists

Transparent pricing structure

Continuous support post-project