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We are proud to work with some of the most innovative life sciences organizations.
The biggest impact that Quality Connect has had on my day-to-day is managing review workflows hassle free, the ease of signing documents, and gaining visibility on the signature process.
Sonette O'Reilly
Document Control Specialist
Montrium’s Validation Accelerator Toolkit for Adobe Sign not only saved us time, but also significantly reduced costs compared to managing and completing the validation process in-house
Flynn Eldred
VP of Quality @ Biovie
The automation of training on SOPs and WIs, in addition to the automated periodic review system, has made a huge difference in our compliance initiatives and quality management processes.
Miya Johnson
Regulatory Affairs Specialist @ Seattle Childrens Hospital
“eTMF Connect is a huge improvement. […] We went from one study to three studies, from one country to several, thereby more than tripling the number of clinical sites. It would not have been possible to scale the way we needed to without eTMF Connect.”
Magali Lurquin
Senior Associate, Regulatory Affairs at Immune Biosolutions
Being able to really feel your impact as an employee is a testament to how much trust and space our leaders give us. We have a "we can do anything" mindset that drives us to produce great things. But at the base of why I love Montrium is the people - they're all brains and all heart.
Alison Robins
Content Marketing Manager
Partnerships are critical to the success of our business. We've built a rich and vibrant partner ecosystem for our customers to take advantage of
Oliver Pearce
Director of Growth @ Montrium
When initially uploading documents and comparing them to the system’s placeholders aligned with the DIA’s TMF Reference Model, right away we could see in the eTMF Connect Navigator what was effectively complete, any documents we were missing, and any titles that needed to be named differently.
Gina Varner
Director of Regulatory Affairs
We’ve seen results in the form of reduced costs, time, and effort relative to training and documenting training. This was previously tracked with Excel spreadsheet training logs. Quality Connect allows one employee to manage the trainings and SOPs.
Maryann Böger
Clinical Systems and Quality Manager
Not only is eTMF Connect a significant tool for sponsors’ trials, but it is also a modern approach for maintaining essential clinical trial documentation by HungaroTrial, as we are able to provide a high-quality, clean, transparent, up-to-date document management system to our clients, which greatly increases work efficiency.
Dr. Mátyás Pethő
Clinical Research Manager
We realized very early on that to scale our Phase II successes in the next step of our journey, bringing in the appropriate technology to support this activity would be key. By partnering with Montrium, we not only leverage a sophisticated and robust eTMF system, but a knowledgeable and dedicated partner in the clinical trial arena.
Amy Emerson
Lykos Therapeutics
We chose to work with Montrium due to their expertise in the regulatory and technology landscape, understanding of our challenges, and quick responsiveness. We had less support when evaluating other companies.
Isabel Brosseau
IT Quality System Owner
Document control can be an extraordinarily complex process, so we looked for a system that could automate as much as possible, while still providing robust oversight and transparency to all involved — and that’s what we found with Montrium.
Patrick Bailey
Director of Quality
We have been extremely pleased with the guidance that we are being provided. We understood that it would be very important for us to find a platform that could grow with us as we progressed into Phase III.
Kimberly Swint
Manager of Clinical Trials Documentation
The biggest impact that Quality Connect has had on my day-to-day is managing review workflows hassle free, the ease of signing documents, and gaining visibility on the signature process.
Sonette O'Reilly
Document Control Specialist
Montrium’s Validation Accelerator Toolkit for Adobe Sign not only saved us time, but also significantly reduced costs compared to managing and completing the validation process in-house
Flynn Eldred
VP of Quality @ Biovie
The automation of training on SOPs and WIs, in addition to the automated periodic review system, has made a huge difference in our compliance initiatives and quality management processes.
Miya Johnson
Regulatory Affairs Specialist @ Seattle Childrens Hospital
“eTMF Connect is a huge improvement. […] We went from one study to three studies, from one country to several, thereby more than tripling the number of clinical sites. It would not have been possible to scale the way we needed to without eTMF Connect.”
Magali Lurquin
Senior Associate, Regulatory Affairs at Immune Biosolutions
Being able to really feel your impact as an employee is a testament to how much trust and space our leaders give us. We have a "we can do anything" mindset that drives us to produce great things. But at the base of why I love Montrium is the people - they're all brains and all heart.
Alison Robins
Content Marketing Manager
Partnerships are critical to the success of our business. We've built a rich and vibrant partner ecosystem for our customers to take advantage of
Oliver Pearce
Director of Growth @ Montrium
When initially uploading documents and comparing them to the system’s placeholders aligned with the DIA’s TMF Reference Model, right away we could see in the eTMF Connect Navigator what was effectively complete, any documents we were missing, and any titles that needed to be named differently.
Gina Varner
Director of Regulatory Affairs
We’ve seen results in the form of reduced costs, time, and effort relative to training and documenting training. This was previously tracked with Excel spreadsheet training logs. Quality Connect allows one employee to manage the trainings and SOPs.
Maryann Böger
Clinical Systems and Quality Manager
Not only is eTMF Connect a significant tool for sponsors’ trials, but it is also a modern approach for maintaining essential clinical trial documentation by HungaroTrial, as we are able to provide a high-quality, clean, transparent, up-to-date document management system to our clients, which greatly increases work efficiency.
Dr. Mátyás Pethő
Clinical Research Manager
We realized very early on that to scale our Phase II successes in the next step of our journey, bringing in the appropriate technology to support this activity would be key. By partnering with Montrium, we not only leverage a sophisticated and robust eTMF system, but a knowledgeable and dedicated partner in the clinical trial arena.
Amy Emerson
Lykos Therapeutics
We chose to work with Montrium due to their expertise in the regulatory and technology landscape, understanding of our challenges, and quick responsiveness. We had less support when evaluating other companies.
Isabel Brosseau
IT Quality System Owner
Document control can be an extraordinarily complex process, so we looked for a system that could automate as much as possible, while still providing robust oversight and transparency to all involved — and that’s what we found with Montrium.
Patrick Bailey
Director of Quality
We have been extremely pleased with the guidance that we are being provided. We understood that it would be very important for us to find a platform that could grow with us as we progressed into Phase III.
Kimberly Swint
Manager of Clinical Trials Documentation
The biggest impact that Quality Connect has had on my day-to-day is managing review workflows hassle free, the ease of signing documents, and gaining visibility on the signature process.
Sonette O'Reilly
Document Control Specialist
Montrium’s Validation Accelerator Toolkit for Adobe Sign not only saved us time, but also significantly reduced costs compared to managing and completing the validation process in-house
Flynn Eldred
VP of Quality @ Biovie
The automation of training on SOPs and WIs, in addition to the automated periodic review system, has made a huge difference in our compliance initiatives and quality management processes.
Miya Johnson
Regulatory Affairs Specialist @ Seattle Childrens Hospital
“eTMF Connect is a huge improvement. […] We went from one study to three studies, from one country to several, thereby more than tripling the number of clinical sites. It would not have been possible to scale the way we needed to without eTMF Connect.”
Magali Lurquin
Senior Associate, Regulatory Affairs at Immune Biosolutions
Being able to really feel your impact as an employee is a testament to how much trust and space our leaders give us. We have a "we can do anything" mindset that drives us to produce great things. But at the base of why I love Montrium is the people - they're all brains and all heart.
Alison Robins
Content Marketing Manager
Partnerships are critical to the success of our business. We've built a rich and vibrant partner ecosystem for our customers to take advantage of
Oliver Pearce
Director of Growth @ Montrium
When initially uploading documents and comparing them to the system’s placeholders aligned with the DIA’s TMF Reference Model, right away we could see in the eTMF Connect Navigator what was effectively complete, any documents we were missing, and any titles that needed to be named differently.
Gina Varner
Director of Regulatory Affairs
We’ve seen results in the form of reduced costs, time, and effort relative to training and documenting training. This was previously tracked with Excel spreadsheet training logs. Quality Connect allows one employee to manage the trainings and SOPs.
Maryann Böger
Clinical Systems and Quality Manager
Not only is eTMF Connect a significant tool for sponsors’ trials, but it is also a modern approach for maintaining essential clinical trial documentation by HungaroTrial, as we are able to provide a high-quality, clean, transparent, up-to-date document management system to our clients, which greatly increases work efficiency.
Dr. Mátyás Pethő
Clinical Research Manager
We realized very early on that to scale our Phase II successes in the next step of our journey, bringing in the appropriate technology to support this activity would be key. By partnering with Montrium, we not only leverage a sophisticated and robust eTMF system, but a knowledgeable and dedicated partner in the clinical trial arena.
Amy Emerson
Lykos Therapeutics
We chose to work with Montrium due to their expertise in the regulatory and technology landscape, understanding of our challenges, and quick responsiveness. We had less support when evaluating other companies.
Isabel Brosseau
IT Quality System Owner
Document control can be an extraordinarily complex process, so we looked for a system that could automate as much as possible, while still providing robust oversight and transparency to all involved — and that’s what we found with Montrium.
Patrick Bailey
Director of Quality
We have been extremely pleased with the guidance that we are being provided. We understood that it would be very important for us to find a platform that could grow with us as we progressed into Phase III.
Kimberly Swint
Manager of Clinical Trials Documentation
The biggest impact that Quality Connect has had on my day-to-day is managing review workflows hassle free, the ease of signing documents, and gaining visibility on the signature process.
Sonette O'Reilly
Document Control Specialist
Montrium’s Validation Accelerator Toolkit for Adobe Sign not only saved us time, but also significantly reduced costs compared to managing and completing the validation process in-house
Flynn Eldred
VP of Quality @ Biovie
The automation of training on SOPs and WIs, in addition to the automated periodic review system, has made a huge difference in our compliance initiatives and quality management processes.
Miya Johnson
Regulatory Affairs Specialist @ Seattle Childrens Hospital
“eTMF Connect is a huge improvement. […] We went from one study to three studies, from one country to several, thereby more than tripling the number of clinical sites. It would not have been possible to scale the way we needed to without eTMF Connect.”
Magali Lurquin
Senior Associate, Regulatory Affairs at Immune Biosolutions
Being able to really feel your impact as an employee is a testament to how much trust and space our leaders give us. We have a "we can do anything" mindset that drives us to produce great things. But at the base of why I love Montrium is the people - they're all brains and all heart.
Alison Robins
Content Marketing Manager
Partnerships are critical to the success of our business. We've built a rich and vibrant partner ecosystem for our customers to take advantage of
Oliver Pearce
Director of Growth @ Montrium
When initially uploading documents and comparing them to the system’s placeholders aligned with the DIA’s TMF Reference Model, right away we could see in the eTMF Connect Navigator what was effectively complete, any documents we were missing, and any titles that needed to be named differently.
Gina Varner
Director of Regulatory Affairs
We’ve seen results in the form of reduced costs, time, and effort relative to training and documenting training. This was previously tracked with Excel spreadsheet training logs. Quality Connect allows one employee to manage the trainings and SOPs.
Maryann Böger
Clinical Systems and Quality Manager
Not only is eTMF Connect a significant tool for sponsors’ trials, but it is also a modern approach for maintaining essential clinical trial documentation by HungaroTrial, as we are able to provide a high-quality, clean, transparent, up-to-date document management system to our clients, which greatly increases work efficiency.
Dr. Mátyás Pethő
Clinical Research Manager
We realized very early on that to scale our Phase II successes in the next step of our journey, bringing in the appropriate technology to support this activity would be key. By partnering with Montrium, we not only leverage a sophisticated and robust eTMF system, but a knowledgeable and dedicated partner in the clinical trial arena.
Amy Emerson
Lykos Therapeutics
We chose to work with Montrium due to their expertise in the regulatory and technology landscape, understanding of our challenges, and quick responsiveness. We had less support when evaluating other companies.
Isabel Brosseau
IT Quality System Owner
Document control can be an extraordinarily complex process, so we looked for a system that could automate as much as possible, while still providing robust oversight and transparency to all involved — and that’s what we found with Montrium.
Patrick Bailey
Director of Quality
We have been extremely pleased with the guidance that we are being provided. We understood that it would be very important for us to find a platform that could grow with us as we progressed into Phase III.
Kimberly Swint
Manager of Clinical Trials Documentation
The biggest impact that Quality Connect has had on my day-to-day is managing review workflows hassle free, the ease of signing documents, and gaining visibility on the signature process.
Sonette O'Reilly
Document Control Specialist
Montrium’s Validation Accelerator Toolkit for Adobe Sign not only saved us time, but also significantly reduced costs compared to managing and completing the validation process in-house
Flynn Eldred
VP of Quality @ Biovie
The automation of training on SOPs and WIs, in addition to the automated periodic review system, has made a huge difference in our compliance initiatives and quality management processes.
Miya Johnson
Regulatory Affairs Specialist @ Seattle Childrens Hospital
“eTMF Connect is a huge improvement. […] We went from one study to three studies, from one country to several, thereby more than tripling the number of clinical sites. It would not have been possible to scale the way we needed to without eTMF Connect.”
Magali Lurquin
Senior Associate, Regulatory Affairs at Immune Biosolutions
Being able to really feel your impact as an employee is a testament to how much trust and space our leaders give us. We have a "we can do anything" mindset that drives us to produce great things. But at the base of why I love Montrium is the people - they're all brains and all heart.
Alison Robins
Content Marketing Manager
Partnerships are critical to the success of our business. We've built a rich and vibrant partner ecosystem for our customers to take advantage of
Oliver Pearce
Director of Growth @ Montrium
When initially uploading documents and comparing them to the system’s placeholders aligned with the DIA’s TMF Reference Model, right away we could see in the eTMF Connect Navigator what was effectively complete, any documents we were missing, and any titles that needed to be named differently.
Gina Varner
Director of Regulatory Affairs
We’ve seen results in the form of reduced costs, time, and effort relative to training and documenting training. This was previously tracked with Excel spreadsheet training logs. Quality Connect allows one employee to manage the trainings and SOPs.
Maryann Böger
Clinical Systems and Quality Manager
Not only is eTMF Connect a significant tool for sponsors’ trials, but it is also a modern approach for maintaining essential clinical trial documentation by HungaroTrial, as we are able to provide a high-quality, clean, transparent, up-to-date document management system to our clients, which greatly increases work efficiency.
Dr. Mátyás Pethő
Clinical Research Manager
We realized very early on that to scale our Phase II successes in the next step of our journey, bringing in the appropriate technology to support this activity would be key. By partnering with Montrium, we not only leverage a sophisticated and robust eTMF system, but a knowledgeable and dedicated partner in the clinical trial arena.
Amy Emerson
Lykos Therapeutics
We chose to work with Montrium due to their expertise in the regulatory and technology landscape, understanding of our challenges, and quick responsiveness. We had less support when evaluating other companies.
Isabel Brosseau
IT Quality System Owner
Document control can be an extraordinarily complex process, so we looked for a system that could automate as much as possible, while still providing robust oversight and transparency to all involved — and that’s what we found with Montrium.
Patrick Bailey
Director of Quality
We have been extremely pleased with the guidance that we are being provided. We understood that it would be very important for us to find a platform that could grow with us as we progressed into Phase III.
Kimberly Swint
Manager of Clinical Trials Documentation
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