How Natural Language Processing (NLP) improves reference creation

Creating references for medical affairs or promotional content can be really slow if done manually. Paige AI, our artificial intelligence assistant, increases the speed of referencing by ten. Paige AI uses Natural Language Processing (NLP) to understand and make sense of human language. She analyses the text you want to link to a reference, deciphers what has been written, and then searches for similar content that has already been used in past references.

Introducing Paige: AI-Assisted References for Life Sciences

Creating references can be a slow and painful process and is a major pain point for a lot of companies. Our team has spent a lot of time researching and developing ways to improve this process. This is why we are thrilled to introduce Paige: AI-assisted references for life sciences. The fastest and most accurate way to reference claims in your content.

How Artificial Intelligence will Transform Medical Affairs and Commercial Teams

Commercial and medical affairs teams in life sciences are undergoing a massive industry transformation. Teams are under pressure to produce more content while maintaining compliance. Artificial Intelligence is the way that repetitive tasks can be learned and executed in a way that gives context to team members. Here are 5 ways medical affairs and life science promotions will be transformed with artificial intelligence. 

The Road to an Efficient Medical, Legal and Regulatory Review Process

An MLR system is vital for an organization to properly manage and prioritize its time. It is important to choose the right platform that will give exceptional long-lasting results. These are key requirements needed for an efficient MLR system.

How Papercurve Wins with Customer Success

One of the major differentiating factors between Papercurve and their competitors is their committed Customer Success Team (CST). With core values like ensuring customer happiness and making software disappear, the Papercurve Customer Success Team is dedicated to helping your team achieve its business goals.

Ace the Audit: Tracing Documents Back to the Source

When life science companies have their content audited, Papercurve is there to help. Knowing who approved the document, when it was released, and what evidence was used to back medical claims is key to meeting audit requirements or satisfying inquiries from public health authorities.‍ Assigning a job number in Papercurve creates traceability to information that an auditor will need.

Papercurve Company Profile: No Fixed Address Inc. Health

The next installment in the Papercurve Spotlight series highlights one of our partner agencies, No Fixed Address Inc. Health.

Helping Speed Up Your Medical Legal Regulatory Review Process

At Papercurve we believe in a set of core values that align with unlocking the most for our clients. Part of our core values involves helping our clients unlock employee efficiency and effectiveness. This is a value we believe sets us apart from our competitors.

Papercurve Company Profile: MedComms Solutions

Welcome to the Papercurve Spotlight series, where we dig into who our customers and partners are and what they are up to. This article highlights one of our partner agencies, MedComms Solutions Inc.

Home-Grown Hope: Canada's contenders for a COVID-19 Vaccine

Without a doubt, COVID-19 has persisted for a lot longer than we had all anticipated. In Canadaalone, we have exceeded 300,000 total cases. Globally, we have surpassed an astonishing 59million cases, with over 1.4 million deaths. As we close in on one year since the pandemicbegan, the question on everyone’s mind is: “When are we getting a vaccine?”

The medical conference is dead. Long live the medical conference.

In just a few months, the coronavirus pandemic has radically disrupted the world of medical conferences. What does this mean for healthcare providers, patient organizations, medical societies, pharmaceutical companies, and health marketing agencies? Let’s explore the significant underlying change drivers and possible long-term implications that COVID-19 has and will have on medical conferences in 2020 and beyond.

“Fake News” and Credibility in Medical Publishing

Doubtlessly, one of the defining phrases of the 2010s is “fake news.” We hear it being thrown around by politicians and celebrities alike, not to mention by social media users when they disagree with a news article or editorial. The Pharma industry is no stranger to fake news either.

Invivo Communications Presents: Covid‑19 and the Science of Soap

As society begins planning to re-open businesses, protecting ourselves and each other from the coronavirus is still a paramount necessity. As we prepare to get back to a “new normal”, it’s important to remember that we’re armed with one of the oldest weapons in human history: SOAP.

If, Then: How To Pivot Your Marketing Strategies During COVID-19

With cancelled conferences, postponed ad schedules and on-hold in-person review meetings, marketing your brand and products during a global pandemic is tough. In this post, we explore some of the key ways Life Sciences and Pharmaceutical companies are pivoting their marketing efforts due to COVID-19 in order to meet the demands of this rapidly-changing climate.

Top 3 Ways To Maximize Remote Working During A Crisis

Due to the COVID-19 outbreak, chances are your team has tested remote access through virtual private access (VPN) and adopted a working-from-home policy. And if you’re fortunate enough, teams already operating from a 100% remote office have not missed a beat in the wake of the pandemic.

How AI and Big Data Will Disrupt Pharma’s Regulatory Compliance Standards ⚙️

The industry as we know it is changing. Pharmaceutical and life sciences companies across the globe are experiencing more pressure than ever to keep up with increased regulatory standards while moving at a pace that requires them to innovate in order to remain competitive. 

Checklist: The all-star method to prepare your content for Medical Legal Regulatory reviews 🏆

Great content is useful and usable. At Papercurve, we understand the lengths it takes to create useful and usable content for pharmaceutical and life sciences companies. From MLR review preparation to revisions, content must go through various stages of the review process before it becomes approved and published. That's why we created a checklist...

How to reduce regulatory bottlenecks and speed up content delivery 🚚

We all face it. Meeting the demands of regulatory standards is important but has the ability to significantly slow us down on our mission to deliver content. It can reduce time to market, conflicts with deadlines and schedules and ultimately drains out content creators and those involved in triaging stakeholder feedback.

Appreciation: The #1 tool for your team in 2020 🙏

We look to the team culture honing experts like Google and LinkedIn to uncover the best characteristics of a winning team. We’ll also look at the ways in which you can leverage these learnings as tools for your marketing team in 2020.

Why folders are no longer the best way to organize your team’s files

We’ve all been there before. Your manager just asked you for a file your predecessor stored in the previous year’s team folder. You try to find the file urgently, rushing through years and years of information only to realize it might take you less time to rewrite the file than try and guess where the file might’ve been stored in the first place. Why? Because organizing files through folders is only intuitive to the person storing them. 

5 highlights from the 2019 PAAB training conference

The Pharmaceutical Advertising Advisory Board, better known as PAAB, had their annual training and information sessions in Montreal and Toronto this week. Here are the top five highlights we gathered from the sessions.

Happy Thanksgiving: The history of life sciences advertising

Thanksgiving is steeped in history, whether it’s the beginnings of the Pilgrims’ harvest meal or that apple pie recipe that has been handed down through your family for generations. This week, we look at the origins of the first drug television ad.

Product Update: Word and PowerPoint Support

We are making it easier to get your content into Papercuve. You can now upload Word and PowerPoint files without converting them to PDF first. This was our most requested feature and we’re excited to roll it out. 

It's time to say goodbye to "Track Changes"

The origins of “Track Changes” in Microsoft Word go back as far as 1986. Over time this feature gained popularity as a way for people to collaborate on documents. But the cloud age has not been kind to Track Changes. Many collaborators working on a single document has caused chaos and a user experience nightmare. It’s time to give up on Track Changes.

Tips for growing your cannabusiness

Wherever your canna-business is located you have opportunities and challenges. New markets are opening up like the State of Illinois in January 2020 and new products are entering the market like edibles, beverages, and topicals in Canada starting Dec 17th. The challenges, however, can be daunting. So how do you help your business thrive in this kind of environment?

Six signs your email-based content approvals are not working

Most of us have used email to review and approve content. Everyone has email and knows how to use it, so how bad can it be? Pretty bad actually. Email approvals have several unseen and potentially costly drawbacks.

How to meet the new Canadian Cannabis Document Retention Regulations

October 17 is more than just topicals, edibles and vaporizers. There are new regulations about document retention rules that impact licensed producers in Canada.

Key takeaways from the Cannabis + Technology conference

Last Friday was the inaugural Cannabis + Technology conference at the Steam Whistle Brewery in Toronto. As cannabis becomes legalized in more and more jurisdictions, technology is innovating the way that producers and governments maintain quality standards, store records, and sell products in a retail environment. Here are 2 key takeaways from Friday’s conference.

5 types of people in your content and compliance review process and how to manage them

You have been through your fair share of internal content reviews as you work on getting things approved. There are patterns in how people approach these reviews. We came up with 5 types of approvers that you'll encounter – and how to deal with them.