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 with research grants, contracts, and loan repayment programs. They bring clarity and simplicity to the medical device industry.
**Expertise & scope**
* Specializes in medical device auditing, including ISO 13485 and MDR.
* Offers expertise in understanding what certification bodies and Notified Bodies look for during audits.
* Assists with internal audit schedules and preparation for stage 1, stage 2, surveillance, and MDR audits.
* Focuses on navigating the NIH grants and funding landscape.
**Reputation / proof points**
* Led over 50 audits as a lead auditor for ISO 13485 and MDR.
* Possesses UKAS witnessed and BSI Certified Lead Auditor credentials.
* Received positive client feedback regarding audit quality and QMS effectiveness.
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 with research grants, contracts, and loan repayment programs. They bring clarity and simplicity to the medical device industry.
**Expertise & scope**
* Specializes in medical device auditing, including ISO 13485 and MDR.
* Offers expertise in understanding what certification bodies and Notified Bodies look for during audits.
* Assists with internal audit schedules and preparation for stage 1, stage 2, surveillance, and MDR audits.
* Focuses on navigating the NIH grants and funding landscape.
**Reputation / proof points**
* Led over 50 audits as a lead auditor for ISO 13485 and MDR.
* Possesses UKAS witnessed and BSI Certified Lead Auditor credentials.
* Received positive client feedback regarding audit quality and QMS effectiveness.
Additional information
The Other Consultants emphasizes a direct approach to communication, recommending LinkedIn messages as the primary method of contact. They also offer an email list for subscribers interested in publications related to medical device quality and regulatory matters. The company's mission is to simplify the complexities within the medical device industry. They are registered with Company Number 10958059 and VAT Number 401616343.
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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Focuses on medical device auditing, including ISO 13485 and MDR.
Source
“Auditing is a mandatory requirement of ISO 13485: 2016, every organisation that produces medical devices has a requirement to undertake audits of their Quality Management System (QMS).”
Certifications & Trust Signals
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Client feedback highlights effective internal audits and QMS performance.
Source
““Just to let you know that 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 seeking auditing support.
- Organizations struggling with in-house auditing competency or resources.
- Researchers and institutions navigating NIH grants and funding.
How engagement typically works
- Direct communication via LinkedIn recommended.
- Email list for regulatory updates.
Typical deliverables
- Internal audit schedule management.
- Preparation for certification and surveillance audits.
- Guidance on ISO 13485 and MDR requirements.
- Consulting on NIH grants and funding.
Good to know
- Best when requiring specialized auditing expertise for medical devices.
- Suitable for entities needing assistance with regulatory compliance and grant navigation.
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
UKAS witnessed and BSI Certified Lead Auditor with experience in ISO 13485 and MDR audits.
Regulatory Experience
Over 50 audits conducted as lead auditor for ISO 13485 and MDR.
Supports IVDR
No
