m
maryleaf

Maryam

@maryleaf
4.9(167)

Level 2

Certified Regulatory ISO and Compliance Expert for Medical and IT and Industries

United States
English
About me
Global Regulatory, Quality, Cybersecurity & ISO Compliance Consultant specializing in Medical Devices, Digital Health & IT Security, supporting all industries worldwide. Expertise: EU MDR/IVDR, MDD to MDR CE, FDA, UKCA, SFDA, ISO 13485, 14971, 27001, 27017, 27018, 27701, 42001, 9001, 14001, 45001, 22000, 17025, 15189, 17024, 17100, 20000-1, 22301, 29993, 31000, SOC 2, HIPAA, GDPR, NIST, PCI DSS, GPSR, HACCP & GMP. Services include QMS/ISMS, technical documentation, risk management, gap assessments, audits, implementation, certification readiness, regulatory submissions & global market access. ... Read more

Skills

m
maryleaf
Maryam
$100/hour
Offline • 
Average response time: 1 hour

See my services

Medical Device Regulatory
I will implement iso 13485 and prepare your medical device company for certification
4.9(51)
IT & Cybersecurity Certification
I will achieve iso 9001 certification with efficient qms
4.9(24)

Want to work on an hourly basis?

Tell Maryam what you need.

$100

/

hour

Portfolio

Work experience

Expert_Medicals

Medical Device Regulatory Affairs, Quality & Digital Health Compliance Consultant

Expert Medicals • Self-employed

Jan 2021 - Present • 5 yrs 9 mos

Provide end-to-end global regulatory, quality, cybersecurity, privacy, and compliance consulting for medical device manufacturers, IVD manufacturers, Software as a Medical Device (SaMD) developers, AI-enabled medical device companies, digital health organizations, healthcare software providers, importers, distributors, OEM/ODM companies, private label brands, and startups. Support product development from concept to commercialization through regulatory strategy, device classification, intended use review, regulatory pathway assessment, CE Marking, EU MDR 2017/745, EU IVDR 2017/746, FDA 21 CFR Part 820 (QMSR), FDA 510(k), De Novo, PMA, UKCA, MHRA, Health Canada, MDSAP, TGA, SFDA, MOHAP, NMPA, PMDA, CDSCO, HSA, NPRA, Swissmedic, and international market access. Provide information security, privacy, and compliance consulting including ISO/IEC 27001, ISO/IEC 27017, ISO/IEC 27018, ISO/IEC 27701, ISO/IEC 20000-1, ISO/IEC 22301, ISO/IEC 42001, SOC 2 Type I & II, HIPAA, HITRUST, PCI DSS 4.0, NIST Cybersecurity Framework (CSF), NIST SP 800-53, CIS Controls, GDPR, Saudi PDPL, UAE Personal Data Protection Law, AI governance, cloud security, and digital compliance frameworks. Develop and review Technical Documentation, Technical Files, Design Dossiers, Device Master Records, General Safety & Performance Requirements (GSPR), Clinical Evaluation Reports (CER), Clinical Evaluation Plans (CEP), Performance Evaluation Reports (PER), Biological Evaluation Reports (BER), Usability Engineering Files, Software Documentation, Software Development Lifecycle (SDLC) documentation, Secure Development documentation, Cybersecurity Risk Management Files, Threat Modeling, Software Bill of Materials (SBOM), Vulnerability Management documentation, Labeling, Instructions for Use (IFU), UDI compliance, EUDAMED readiness, Declaration of Conformity, Essential Requirements, technical dossiers, cybersecurity privacy, and global market access solutions from concept through commercialization.

167 Reviews
4.9

(162)
(2)
(1)
(1)
(1)
Rating Breakdown
  • Seller communication level
    4.9
  • Quality of delivery
    4.9
  • Value of delivery
    4.9
1-5 out of 167 Reviews
Sort By
Most relevant
    A
    image-docs

    alifatemiardeka

    US

    United States

    5

    Amazing job! Professional- thank you!

    $600-$800

    Price

    8 days

    Duration

    gig

    FDA & Food Safety Clearance

    Helpful?
    Yes
    No
    S

    s_p_d_orcaa

    AU

    Australia

    5

    punctual, reviewing now.

    $50

    Price

    3 days

    Duration

    gig

    Medical Device Regulatory

    Helpful?
    Yes
    No
    F

    felixvane

    US

    United States

    5

    She demonstrated exceptional expertise in ISO 13485 and medical device quality management systems. The guidance provided was practical, well-structured, and reflected genuine hands-on experience with regulatory compliance and certification preparation.

    $100-$200

    Price

    4 days

    Duration

    gig

    Product Consultation

    Helpful?
    Yes
    No
    L

    lyra_belrosee

    US

    United States

    5

    Excellent experience working with Maryam. She demonstrated strong knowledge of ISO 9001 requirements and provided practical, well-structured guidance that was easy to understand and implement. Communication was professional, responsive, and timely throughout the project. The deliverables were detailed,...

    $50

    Price

    2 days

    Duration

    gig

    IT & Cybersecurity Certification

    Helpful?
    Yes
    No
    J

    jaxon_wilde0

    US

    United States

    5

    Very good work! The quality management documents were created in a clean and professional way. Everything was reliable and well structured. You can clearly see that he truly loves his work and is very committed. Highly recommended! 👍

    $100-$200

    Price

    4 days

    Duration

    gig

    Product Descriptions

    Helpful?
    Yes
    No