Compliance Audit Services — SOC 2, ISO 27001, HIPAA, GDPR | CertPro CPA LLC

Every Framework.
One Audit Partner.

CertPro delivers independent third-party compliance audits across 20+ frameworks — SOC 2, ISO 27001, HIPAA, GDPR, ISO 42001, and beyond. We scope it, audit it, and issue the certificate ourselves as a licensed CPA firm.

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97%
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SOC 2 — Issued
ISO 27001 — Issued
HIPAA — In Progress
SOC 2
SOC

SOC 2 Type I & II

Formal SOC 2 attestation issued directly by CertPro as a licensed CPA firm. We scope, remediate, and issue — no middleman. Accepted by AWS, Salesforce AppExchange and enterprise procurement worldwide.

Type I: 4–8 wksSaaS, Cloud, FintechUS / Global
27001
ISO

ISO 27001:2022

IAF-accredited ISMS certification. 80% pre-built policy library, gap analysis, and certification audit — all in one engagement. The global standard required by EU, Middle East, and APAC enterprise buyers.

8–16 weeksAll sectorsGlobal
42001
ISO · AI

ISO 42001:2023

The world's first AI Management System standard. Certify your AI governance framework before regulators require it. Relevant for any company building, deploying, or procuring AI systems.

8–14 weeksAI / ML companiesGlobal
27701
ISO

ISO 27701:2019

Privacy extension to ISO 27001. Certifies your PIMS against GDPR and global privacy requirements. Required by enterprise DPA frameworks and EU data protection authorities.

8–12 weeksData controllers / processorsGlobal
27018
ISO

ISO 27018:2019

PII protection standard for public cloud environments. Covers data deletion, transparency, and consent controls beyond ISO 27001. Increasingly required by enterprise cloud procurement.

6–10 weeksCloud & IaaS providersGlobal
HIPAA
Privacy

HIPAA Compliance Assessment

Independent audit of administrative, physical, and technical safeguards. Produces the formal report healthcare clients need before signing a BAA — not a self-assessment checklist.

6–12 weeksHealthcare & HealthTechUSA
GDPR
Privacy

GDPR Compliance Audit

Data mapping, DPIA execution, lawful basis assessment, controller/processor gap review, and a readiness report your DPO can act on. Applies to any org processing EU personal data.

6–10 weeksAll sectorsEU & Global
CCPA
Privacy

CCPA / CPRA Compliance

Data inventory, opt-out mechanism review, consumer rights workflow audit, and a gap report tied to CPRA obligations. Covers the original CCPA and 2023 CPRA amendments.

4–8 weeksConsumer-facing businessesUSA
PIPEDA
Privacy

PIPEDA Compliance

Canada's federal privacy law for commercial activity. Assessment covers fair information principles, consent obligations, breach notification requirements, and accountability framework documentation.

4–8 weeksCanadian businessesCanada
9001
Quality

ISO 9001:2015

Quality Management System certification for companies demonstrating process consistency to enterprise customers or government contracts. Documented QMS development and third-party certification audit.

8–16 weeksAll sectorsGlobal
14001
Quality

ISO 14001:2015

Environmental Management System certification. Demonstrates your commitment to environmental responsibility, regulatory compliance, and continuous improvement — required by many enterprise supply chains.

8–14 weeksAll sectorsGlobal
45001
Quality

ISO 45001:2018

Occupational Health & Safety Management System standard. Reduces workplace incidents, meets legal obligations, and demonstrates duty of care to employees and enterprise procurement teams.

8–14 weeksAll sectorsGlobal
22301
Quality

ISO 22301:2019

Business Continuity Management System certification. Demonstrates your organisation can maintain critical functions during disruptions — required by financial sector, government, and enterprise vendor frameworks.

8–14 weeksAll sectorsGlobal
20000
Quality

ISO 20000-1:2018

IT Service Management System certification. The international standard for ITSM — demonstrates structured, reliable IT service delivery. Required by many government and enterprise IT contracts globally.

8–14 weeksIT service providersGlobal
CE
Specialized

CE Marking

Mandatory EU conformity for electronics, machinery, medical devices, and software with hardware components. We handle technical documentation, conformity assessment, and Declaration of Conformity issuance.

4–12 weeksHardware & devicesEU / EEA
13485
Specialized

ISO 13485:2016

Medical device Quality Management System standard. Required for manufacturers and suppliers in the medical device industry globally — mandatory for EU MDR compliance and FDA quality system requirements.

10–18 weeksMedical device industryGlobal
21001
Specialized

ISO 21001:2018

Educational Organization Management System standard. Demonstrates structured, learner-focused management for educational institutions, training providers, and e-learning platforms seeking enterprise or government contracts.

8–14 weeksEducation & trainingGlobal
41001
Specialized

ISO 41001:2018

Facility Management System standard. Certifies structured delivery of FM services across real estate, infrastructure, and workplace management — required by large enterprise FM procurement frameworks.

8–14 weeksFacility managementGlobal
How It Works

Four Steps from Scope to Certificate

Every engagement follows the same structured methodology — no surprises, no scope creep, no vague deliverables.

1
Step 01

Scoping

We define which systems, people, and processes fall inside the audit boundary. You get a written project plan with fixed milestones before we start.

Day 1–3
2
Step 02

Gap Analysis

A control-by-control review against your target standard. Every gap is documented with a severity rating, remediation effort estimate, and owner assignment.

Week 1–3
3
Step 03

Remediation

We provide 80% pre-built policy and procedure templates. Your team implements — we review, advise, and approve before the formal audit begins.

Week 3–6
4
Step 04

Audit & Issuance

Formal evidence collection, testing, and audit report or certificate issuance. IAF-accredited for ISO. AICPA-compliant for SOC 2. Accepted globally.

Certified!
FAQ

Compliance Questions, Answered

Specific answers to the questions clients ask before, during, and after an audit engagement — not generic compliance marketing copy.

It depends on three things: who your customers are, where they're based, and what they're asking for. SOC 2 is primarily driven by US enterprise SaaS buyers. ISO 27001 is required by EU, Middle East, and APAC enterprise customers. HIPAA applies if you handle US healthcare data. GDPR applies if you process EU personal data. Most fast-growing companies need more than one. In a 30-minute scoping call, we'll tell you exactly what applies to your situation — no guesswork.
SOC 2 Type I: 4–8 weeks from kickoff to report. SOC 2 Type II: 6–12 months total (includes the mandatory observation period). ISO 27001: 8–16 weeks from gap analysis to IAF-accredited certificate. HIPAA assessment: 6–12 weeks. GDPR readiness: 6–10 weeks. These ranges assume normal organizational responsiveness. Clients who engage their teams quickly and use our pre-built documentation kits land at the lower end of each range.
Compliance is self-declared — you've implemented controls and believe you meet a standard. Certification means an independent, licensed third party has tested those controls and issued a formal report or certificate. Enterprise procurement, cyber insurance underwriters, and regulators require the latter. A self-completed compliance questionnaire does not substitute for an independent audit report.
Yes — and we recommend it. SOC 2 and ISO 27001 share approximately 70% of their control requirements. We design combined audit programs that reuse evidence, policy documents, and control tests across both frameworks. Clients pursuing both together typically reduce total effort by 35–50% compared to running them as separate sequential engagements. We scope this explicitly in our project plans.
Compliance platforms automate evidence collection and readiness tracking — they are useful tools. But they cannot issue SOC 2 attestation reports or ISO 27001 certificates. Those require a licensed auditor. CertPro is that auditor. Many of our clients use a compliance platform alongside our audit services. We're platform-agnostic and work with clients on any tooling setup — or with no tooling at all.
No. Most clients engage us before they have a mature control environment — that's exactly why they need a gap analysis. We assess where you are, identify what's missing, help you build it, and then audit it. Coming in early gives us time to design controls properly rather than retrofitting them before an audit deadline.
We work with SaaS companies, cloud infrastructure providers, healthcare IT vendors, fintech platforms, AI/ML companies, legal tech firms, and enterprise software businesses across 25+ countries. Company size ranges from Series A startups to publicly listed enterprises. The common thread is that their customers or regulators require independent third-party compliance validation.
For SOC 2: a formal Type I or Type II attestation report issued under SSAE 18 by CertPro as a licensed CPA firm. For ISO 27001 and other ISO standards: an IAF-accredited certificate from a recognized certification body, plus the audit report. For HIPAA/GDPR: a detailed compliance assessment report documenting your control environment, identified gaps, risk ratings, and recommended remediation actions. All reports are attorney-shareable and enterprise-grade.
Type I is a point-in-time report — it says your controls were suitably designed as of a specific date. Type II covers an observation period (typically 6–12 months) and tests whether those controls actually operated effectively throughout. Enterprise customers almost always require Type II. Type I is useful as a milestone on the way to Type II, or when a customer specifically requests it for an initial vendor onboarding.
CertPro issues the report directly. We are a licensed CPA LLC enrolled in the AICPA Peer Review program, which means we can issue SOC 2 attestation reports under SSAE 18 — the same standard used by Deloitte, PwC, and KPMG. You do not need a separate CPA firm. Our reports are accepted by the same enterprise procurement teams that accept Big 4 reports.
Security (Common Criteria) is mandatory — all SOC 2 reports include it. Availability, Confidentiality, Processing Integrity, and Privacy are optional, chosen based on your service commitments and what your customers are asking for in security questionnaires. We review your customer agreements and security questionnaire responses during scoping to determine the right criteria — you don't have to guess.
Scope covers the systems, infrastructure, people, and third-party services that directly support delivery of your service commitments. Typically: your production application and database, cloud infrastructure (AWS, GCP, Azure), CI/CD pipeline, identity and access management, and key subservice organizations. We define scope precisely during the scoping phase — too broad wastes audit effort; too narrow creates gaps your customers will raise in questionnaires.
SOC 2 Type II reports cover a defined period — typically 12 months. Enterprise customers expect an annual report with no gap in coverage. You'll need a new Type II audit each year. Annual renewals are faster and less expensive than the initial audit because your controls, evidence collection, and audit processes are already established. CertPro offers annual renewal engagements on fixed-fee terms.
Your SOC 2 report typically replaces or shortens the security questionnaire process with customers. Many enterprise procurement teams accept a SOC 2 Type II report in lieu of a completed vendor questionnaire. For questionnaires that still require completion, your SOC 2 report provides pre-validated answers for the majority of security controls — significantly reducing the time your team spends on individual customer security reviews.
Legally voluntary in most jurisdictions — but contractually required by an increasing number of enterprise buyers, particularly in the EU, UK, Saudi Arabia, UAE, and APAC. It appears as a mandatory requirement in government procurement tenders, financial sector vendor due diligence frameworks, and large enterprise supplier policies. For companies doing business outside North America, it is functionally necessary to compete for enterprise contracts.
Our ISO 27001 gap analysis reviews your current controls, policies, and processes against all 93 Annex A controls in ISO 27001:2022 and the mandatory clauses (4–10). Each control is assessed as fully implemented, partially implemented, or not implemented. You receive a gap report with severity ratings, remediation effort estimates, responsible owner suggestions, and our 80% pre-built policy and procedure kit covering the most common gaps.
Three years. Annual surveillance audits in years one and two verify your ISMS continues to operate effectively. A full recertification audit is required in year three. Surveillance audits are significantly lighter than the initial certification — they focus on a subset of controls and any non-conformities from the previous cycle. CertPro handles all stages: initial certification, surveillance, and recertification.
ISO 42001:2023 is the first international standard for AI Management Systems — covering how AI is developed, deployed, and governed responsibly. It's most immediately relevant for companies selling AI-powered products to enterprise customers, regulated industries using AI in decision-making, and companies subject to the EU AI Act. Early certification is a genuine differentiator today; in 2–3 years it will likely become a contractual requirement in the same way ISO 27001 has.
ISO 27701 is a privacy extension to ISO 27001, adding a Privacy Information Management System (PIMS). It maps directly to GDPR obligations for both controllers and processors — data subject rights, consent management, cross-border transfer mechanisms, and accountability records. You need it when enterprise customers or EU data protection authorities require documented evidence of a structured privacy governance program.
Yes — and it's more efficient. Both standards share the majority of their control requirements around access management, incident response, asset management, risk assessment, and supplier security. We structure combined engagements so that gap analysis, remediation, and evidence collection serve both audits simultaneously. Clients typically save 35–50% of total effort compared to sequential separate engagements.
Yes. GDPR has explicit extraterritorial scope. It applies to any organization that processes personal data of EU residents — regardless of where the organization is headquartered or where servers are located. If you have EU customers, users, employees, or even website analytics from EU visitors, GDPR obligations apply. Maximum penalties are €20 million or 4% of global annual turnover.
There is no government-issued HIPAA certification — the HHS does not issue certificates. What exists is a HIPAA compliance assessment: an independent audit of your administrative safeguards, physical safeguards, and technical safeguards. CertPro issues a formal assessment report documenting your control environment — this is what healthcare organizations require before signing a Business Associate Agreement with you.
A Business Associate Agreement (BAA) is a contract required by HIPAA between a covered entity and any vendor that creates, receives, maintains, or transmits Protected Health Information on their behalf. If you provide SaaS, cloud storage, analytics, IT services, or any other service where you could potentially access PHI, you are a business associate and must sign BAAs.
A Data Protection Impact Assessment (DPIA) is required under GDPR Article 35 when processing is "likely to result in a high risk" to individuals' rights and freedoms. Mandatory scenarios include: large-scale processing of special category data, systematic profiling, monitoring of publicly accessible areas, and use of new technologies. DPIAs must be completed before the processing begins.
Yes — CCPA applies based on whose data you process, not where you're located. It applies to for-profit businesses that: have annual gross revenues over $25M, process the personal data of 100,000+ California consumers or households annually, or derive 50%+ of revenue from selling consumers' personal data. Fines are $2,500 per unintentional violation and $7,500 per intentional violation.
Yes. GDPR and CCPA share significant overlap in data inventory requirements, privacy notice obligations, data subject/consumer rights, and breach notification. We conduct combined privacy assessments that address both simultaneously. Findings are mapped to each regulation's specific requirements. If you're also pursuing ISO 27701, we align the assessment to that standard at the same time — one assessment covering three frameworks.
Four phases with fixed deliverables at each stage. (1) Scoping: we review your systems, define the audit boundary, assign a dedicated CPA and lead auditor, and issue a written project plan with milestone dates. (2) Gap Analysis: control-by-control review against your target standard. (3) Remediation: we provide pre-built policy templates, review your implementations, and confirm readiness before the formal audit. (4) Formal Audit: evidence collection, testing, and issuance of your attestation report or certificate.
Fixed-fee, project-based pricing — not hourly billing. Your fee is set before the engagement starts and does not change unless scope changes. We provide a detailed written quote after the scoping call based on framework, audit scope, organization size, and complexity. No surprise invoices. Most clients find our pricing 40–60% below comparable Big 4 or regional CPA firm engagements, with no difference in report format, credibility, or AICPA/IAF compliance.
4-hour response guaranteed during business hours. Our team operates across Newark, DE (USA) and Bangalore, India, giving near-round-the-clock coverage across US and European time zones. Every client gets a named CPA, a named lead auditor, and a dedicated communication channel.
Because we run a thorough gap analysis and remediation phase before the formal audit, the large majority of our clients pass on the first attempt — with 80%+ of gaps closed before audit day. In cases where non-conformities are identified during the audit, we work through the corrective action process with you at no additional advisory cost.
Annual surveillance audits, recertification engagements, scope expansion for new products or geographies, and advisory when standards are revised. We also assist with security questionnaire responses that reference your certification scope. Ongoing support is available on a retainer or per-engagement basis.
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Schedule a free 30-minute scoping call with a CertPro expert. We'll identify the right framework, estimate your timeline, and give you a clear roadmap — no commitment required.

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