The Other Consultants
The Other Consultants is a provider of consulting services focused on navigating the National Institutes of Health (NIH) grants and funding landscape. They assist researchers and institutions in understanding and accessing research grants, contracts, and loan repayment programs.
The Other Consultants specializes in guiding clients through the complex world of biomedical research funding, particularly through the National Institutes of Health (NIH). As a key player in the prrc_service directory, they leverage their expertise to help organizations understand the NIH's extensive grant and funding opportunities. Their services encompass assisting clients in identifying suitable funding avenues, understanding the intricacies of the grants process from planning and application to award and post-award reporting. They are adept at interpreting NIH policies and procedures, ensuring clients can effectively manage compliance and oversight requirements. The Other Consultants are committed to providing the necessary support for researchers and institutions to secure vital funding, thereby advancing scientific integrity and public accountability within the biomedical research community. They act as a crucial interface, simplifying the federal landscape for investigators and their institutions.
About
**Who they are**
The Other Consultants is a provider of consulting services focused on navigating the National Institutes of Health (NIH) grants and funding landscape, assisting researchers and institutions in understanding and accessing research grants, contracts, and loan repayment programs. They bring clarity and simplicity to the medical device industry.
**Expertise & scope**
* Specializes in auditing services for medical devices, including ISO 13485 and MDR audits.
* Possesses expertise as a UKAS witnessed and BSI Certified Lead Auditor with over 50 audits conducted.
* Understands the requirements of certification bodies (CBs) and Notified Bodies (NBs).
* Assists with internal audit schedules and preparation for stage 1, stage 2, surveillance, and MDR audits.
**Reputation / proof points**
* Experienced lead auditor with over 50 audits conducted for ISO 13485 and MDR.
* Received positive feedback from clients, including a PRRC of a IIa medical device manufacturer and a Class IIb medical device manufacturer.
The Other Consultants is a provider of consulting services focused on navigating the National Institutes of Health (NIH) grants and funding landscape, assisting researchers and institutions in understanding and accessing research grants, contracts, and loan repayment programs. They bring clarity and simplicity to the medical device industry.
**Expertise & scope**
* Specializes in auditing services for medical devices, including ISO 13485 and MDR audits.
* Possesses expertise as a UKAS witnessed and BSI Certified Lead Auditor with over 50 audits conducted.
* Understands the requirements of certification bodies (CBs) and Notified Bodies (NBs).
* Assists with internal audit schedules and preparation for stage 1, stage 2, surveillance, and MDR audits.
**Reputation / proof points**
* Experienced lead auditor with over 50 audits conducted for ISO 13485 and MDR.
* Received positive feedback from clients, including a PRRC of a IIa medical device manufacturer and a Class IIb medical device manufacturer.
Additional information
The Other Consultants focuses on bringing clarity and simplicity to the medical device industry, particularly concerning auditing and regulatory compliance. They emphasize the mandatory nature of ISO 13485:2016 audits and address common challenges organizations face, such as a lack of in-house competency, difficulties demonstrating independence and objectivity, and resource constraints for effective internal audits. They also highlight cultural issues that can arise when staff audit colleagues and the impact of delayed audit schedules. Their services are designed to support organizations in meeting these critical compliance requirements.
Key Highlights
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Led over 50 audits as a lead auditor for ISO 13485 and MDR.
Source
“I have conducted over 50 audits as the lead auditor for ISO 13485 and MDR.”
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Possesses UKAS witnessed and BSI Certified Lead Auditor credentials.
Source
“I'm a United Kingdom Accreditation Service (UKAS) witnessed and BSI Certified Lead Auditor.”
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Understands the expectations of certification bodies and Notified Bodies.
Source
“I understand what certification bodies (CBs) and Notified Bodies (NBs) look for.”
Certifications & Trust Signals
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Client feedback indicates strong internal audits and effective QMS.
Source
“today’s audit on design didn’t raise any CARs, they accepted that we had a strong internal audit conducted and that our QMS was working and flagging issues”
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Company Number: 10958059
Source
“Company Number: 10958059”
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VAT Number: 401616343
Source
“VAT Number: 401616343”
Buyer Snapshot
Best for
- Medical device manufacturers struggling with internal audit competency.
- Organizations needing support with ISO 13485 and MDR audit preparation.
- Companies seeking to improve their Quality Management System (QMS) auditing processes.
How engagement typically works
- Direct messaging via LinkedIn is the preferred contact method.
- Offers an email list for publications on medical device quality & regulatory topics.
Typical deliverables
- Internal audit schedule management.
- Support for Stage 1, Stage 2, and surveillance audits.
- Guidance on meeting Notified Body and Certification Body expectations.
Good to know
- Best when organizations require specialized auditing expertise to supplement internal resources.
HQ:
London, US
Languages:
English
Timezones:
Europe/London
Claim status:
Listed
Services & Capabilities
PRRC MDR (EU MDR) | PRRC Medical Device Service | Compare Providers & Get Quotes
Jurisdictions:
EU
Industries:
Medical devices, IVD, SaMD, Manufacturing
Portfolio:
6-25
Onboarding time:
5–21 days
Pricing model:
Retainer
Starting from:
GBP 1,800
Included services:
PRRC appointment support, Lifecycle compliance oversight, Change-impact escalation, PMS/vigilance coordination support
Named PRRC:
Yes
Device Classes Supported:
Class IIa, Class IIb
PRRC Qualification Summary:
I provide Person Responsible for Regulatory Compliance (PRRC) services tailored to meet the needs of medical device manufacturers of all sizes.
Additional prrc_service Details
Included Services Detailed
Appointment and mandate support for outsourced PRRC coverage (seed scope), Lifecycle compliance oversight aligned to Article 15 activities (seed scope), Change-impact triage and escalation support (seed scope), Periodic compliance reporting to management (seed scope)
Excluded Services
Notified Body decision-making on conformity assessment, Acting as Legal Manufacturer unless separately contracted, Commercial distribution or importer/distributor operations
Onboarding Steps
Contact via direct message on LinkedIn is the primary method.
Coverage Details
PRRC availability set to Business hours with defined escalation path (seed summary).
Device Classes Supported
IIa, IIb
Supports MDR
Yes
PRRC Qualification Summary
BSI Certified Lead Auditor with extensive experience in ISO 13485 and MDR audits.
Regulatory Experience
Over 50 audits conducted as lead auditor for ISO 13485 and MDR.
Supports IVDR
No
