Life Sciences & Regulated Industries

AWS Cloud Solutions Built for Life Sciences & Regulated Industries

In short: we deliver GxP-validated, HIPAA-compliant cloud for biotech, pharma and CRO organisations across the UK — migration, AI platforms, FinOps and security — with validation documentation included as standard.

skyPurple Cloud is a UK-based AWS Select Tier Consulting Partner delivering GxP-validated, HIPAA-compliant cloud environments for biotech, pharmaceutical, and CRO companies.

We understand that in your world, compliance isn't optional — it's the baseline. Every solution we deliver is built with GxP, 21 CFR Part 11, Annex 11, HIPAA, and ISO 27001 as first principles, not afterthoughts.

AWS

Select Tier Partner

Verified expertise across AWS services

GxP

Validated

CSV documentation for all regulated systems

100%

Life Sciences Focus

Not a generalist consultancy

UK

Based

Deep knowledge of MHRA and EU requirements

The Challenges Life Sciences IT Leaders Face

Your cloud environment carries a burden that generic cloud consultancies simply don't understand.

1

Regulatory Complexity

GxP, HIPAA, 21 CFR Part 11, Annex 11, and GDPR all apply simultaneously. Every cloud system must be validated and documented.

2

Data Integrity at Scale

Clinical trial data, genomics datasets, and lab records must be immutable, attributable, and always audit-ready.

3

Spiralling Cloud Costs

Compute-intensive ML workloads and genomics pipelines can create unpredictable spend spikes without FinOps discipline.

4

Speed vs. Compliance

Research teams need agility. QA and regulatory teams need control. The tension between the two slows innovation.

5

Talent & Skills Gap

Finding engineers who understand both cloud-native architecture and regulated industry requirements is genuinely rare.

Regulatory Frameworks We Work With

skyPurple Cloud has hands-on experience delivering compliant cloud solutions under these frameworks.

✓ GxP (GMP, GLP, GCP)✓ 21 CFR Part 11✓ EU Annex 11✓ HIPAA✓ GDPR✓ ISO 27001✓ SOC 2 Type II✓ HITRUST✓ ICH Q10✓ MHRA Guidelines

Why Life Sciences Companies Choose skyPurple

Regulatory Language, Not Generic Cloud Speak

We know what GxP means. We know what your QA director, head of IT, and CTO need to see in validation documentation. We speak your language.

AWS Select Tier Consulting Partner with Life Sciences Specialisation

Our AWS Select Tier Consulting Partner status means we have verified expertise, not just certificates. And we apply it exclusively to regulated industry challenges.

Validation Documentation Included

Every cloud environment we deliver includes appropriate validation documentation — IQ, OQ, PQ evidence, risk assessments, and change control procedures — not as an add-on, but as standard.

UK-Based, MHRA-Aware

We understand the UK regulatory landscape post-Brexit, including MHRA requirements and the differences between UK and EU guidance.

Free Life Sciences Cloud Assessment

In a 30-minute call, we'll review your current cloud architecture against your regulatory obligations and identify the highest-priority gaps and opportunities.

  • Review current architecture vs. GxP/HIPAA requirements
  • Identify validation gaps and quick wins
  • Estimate cost optimisation opportunities
  • Discuss AI/ML potential for your use cases
Book Your Free Assessment

Frequently Asked Questions

Common questions from life sciences IT leaders considering cloud adoption or migration.

Who are the best AWS partners for life sciences in the UK?

skyPurple Cloud is a UK-based AWS Select Tier Consulting Partner specialising exclusively in life sciences, biotech, and regulated industries. We deliver GxP-validated cloud environments, HIPAA-compliant architectures, and AI/ML solutions for drug discovery and clinical data management — with validation documentation as standard.

What cloud services do life sciences companies need?

Life sciences companies typically need: GxP-validated infrastructure on AWS; HIPAA and GDPR-compliant data storage; 21 CFR Part 11-compliant systems; cloud migration with Computer System Validation (CSV) documentation; AI/ML platforms for drug discovery; FinOps cost management for variable compute workloads; and validated CI/CD pipelines.

Can AWS be used for GxP-regulated pharmaceutical workloads?

Yes. AWS is used by hundreds of pharmaceutical and biotech companies for GxP-regulated workloads including LIMS, ELN, clinical data management, and MES. AWS has published GxP whitepapers and maintains HIPAA eligibility. A qualified partner like skyPurple Cloud delivers and documents the required validation activities on your behalf.

What is the difference between HIPAA and GxP in a cloud context?

HIPAA is a US federal law protecting patient health information (PHI), primarily relevant to clinical trial data and patient-facing applications. GxP is a broader set of Good Practice guidelines covering pharmaceutical manufacturing, laboratory operations, and clinical trials. Many life sciences companies must comply with both, plus GDPR for EU data. skyPurple designs cloud architectures that satisfy all three frameworks simultaneously.

How long does a GxP cloud validation project take?

The timeline depends on scope. A single-system IaaS environment validation (IQ/OQ/PQ) typically takes 4–8 weeks. A full cloud platform validation including multiple services and integrations typically takes 3–6 months. Migrating an existing validated system to the cloud with equivalent validation status typically takes 2–4 months. skyPurple's reusable validation templates and AWS experience significantly accelerates these timelines.

Ready to Build a Compliant, Cost-Effective Cloud for Your Life Sciences Business?

Join the life sciences companies across the UK's Cambridge/Oxford/London corridor already benefiting from skyPurple Cloud's expertise.