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 specialize in bringing clarity and simplicity to the medical device industry.
**Expertise & scope**
* Expertise in navigating the NIH grants and funding landscape.
* Assistance with research grants, contracts, and loan repayment programs.
* Specialized consulting for the medical device industry.
* Focus on medical device auditing, including ISO 13485 and MDR requirements.
* Experience with UKAS witnessed and BSI Certified Lead Audits.
**Reputation / proof points**
* Conducted over 50 audits as lead auditor for ISO 13485 and MDR.
* Understands the requirements of certification bodies (CBs) and Notified Bodies (NBs).
* Received positive feedback from a PRRC of a IIa medical device manufacturer regarding internal audit strength and QMS effectiveness.
* Received positive feedback from 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 with research grants, contracts, and loan repayment programs. They specialize in bringing clarity and simplicity to the medical device industry.
**Expertise & scope**
* Expertise in navigating the NIH grants and funding landscape.
* Assistance with research grants, contracts, and loan repayment programs.
* Specialized consulting for the medical device industry.
* Focus on medical device auditing, including ISO 13485 and MDR requirements.
* Experience with UKAS witnessed and BSI Certified Lead Audits.
**Reputation / proof points**
* Conducted over 50 audits as lead auditor for ISO 13485 and MDR.
* Understands the requirements of certification bodies (CBs) and Notified Bodies (NBs).
* Received positive feedback from a PRRC of a IIa medical device manufacturer regarding internal audit strength and QMS effectiveness.
* Received positive feedback from a Class IIb medical device manufacturer.
Additional information
The Other Consultants emphasizes a direct approach for communication, recommending LinkedIn messages as the primary method of contact. They also offer an email list for subscribers interested in publications covering medical device quality and regulatory topics. Their mission is to simplify complex aspects of the medical device industry, including auditing, PRRC services, and CE Marking.
Key Highlights
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Conducted over 50 audits as 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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Expertise in UKAS witnessed and BSI Certified Lead Audits.
Source
“I'm a United Kingdom Accreditation Service (UKAS) witnessed and BSI Certified Lead Auditor.”
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Understands what certification bodies (CBs) and Notified Bodies (NBs) look for.
Source
“I understand what certification bodies (CBs) and Notified Bodies (NBs) look for.”
Certifications & Trust Signals
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Received positive feedback on internal audit strength and QMS effectiveness from a Class IIa medical device manufacturer.
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” PRRC of a IIa medical device manufacturer.”
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Received positive feedback from a Class IIb medical device manufacturer.
Source
“"Thanks for the immaculate work, Adam" Class IIb medical device manufacturer.”
Buyer Snapshot
Best for
- Medical device manufacturers seeking auditing expertise.
- Organizations needing assistance with NIH grants and funding.
- Companies looking to improve their Quality Management System (QMS).
How engagement typically works
- Direct communication via LinkedIn.
- Email list for regulatory updates.
Typical deliverables
- Medical device audits (ISO 13485, MDR).
- Guidance on NIH grants and funding.
- Consulting on research grants, contracts, and loan repayment programs.
- Support for CE Marking.
Good to know
- Best when direct communication is preferred.
HQ:
London, US
Languages:
English
Timezones:
Europe/London
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
No specific onboarding steps mentioned.
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
