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Getting ready for Facebook pharma changes

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Post with LiveWorld view of how pharma companies need to prepare for changes to the rules about public commenting on Facebook Pages.Facebook has decided to no longer allow pharma companies to “whitelist” their Pages.

What this means: Up until now, pharma companies with Facebook Pages could request that Facebook disable the ability for people to comment on and/or Like brand posts. This exception should not be confused with the ability every Page has to disable the capability for fans to originate a post. Even where Pages do not allow fans to post, people can comment on the Page owner’s posts (unless they have requested and received such an exception). You can read a really good explanation of the difference at Jonathan Richman’s Dose of Digital site.

The only Pages still eligible to request a commenting exception are branded Pages for prescription drugs or non-branded Pages centered on a disease state for which only one prescribed treatment exists. As of August 15, 2011, other Facebook Pages (even those previously eligible for exception — such as disease state Pages and OTC product Pages, like NyQuil) will see the comment and Like capabilities appear for fans.

Planning for interaction

For those companies who’ve had comments disabled to this point, and who’re no longer eligible for the exception, it’s essential to be prepared for the change. The truth is that, given FDA regulations, companies will need either to put well-planned Facebook moderation in place, or terminate their Pages. Because of the obligation to report adverse events (untoward experiences people have with a pharma product), certainly there’s no option not to moderate.

For all pharma companies planning to run Facebook Pages around OTC products or disease states, the resources required for running a Page are now quite different. It will no longer be enough to simply publish information to the Wall — a glorified digital brochure, really. Instead, companies need to be thinking about moderation of undesirable content like spam and profanity, about dealing with comments describing adverse events or off-label use, and ideally, about providing knowledgeable brand representatives who engage in a meaningful, helpful way with people who comment on their Pages.

The opportunity

At LiveWorld, we’ve been thinking about best practices for pharma for some time. Online venues are now and increasingly will be a major source of health information, sharing of experience, and support. This is a very good thing for a number of reasons: It’s good for people to be able to talk with each other about their experience living with health issues. It’s good for pharma and healthcare providers to hear from the people who are using their products. It’s good for people to get reliable information from experts.

While it’s understandable that pharma companies are nervous about the legal implications of people talking about their products, it’s also a great opportunity. Pharma can support all the potentially positive dynamics by allowing people to benefit from the company’s considerable knowledge base, by responding to users who bring forward issues and questions, and by providing a venue for connection among people who use their products and may be dealing with similar life experiences. Plus, they’ll learn a lot from their customers.

People will always talk

Regardless of whether pharma companies decide to keep their Facebook Pages, people will find places to talk to each other about their experiences with particular products and disease states. If companies hold back on providing such conversational venues because of fear of legal liability, the public loses benefits the company can offer, and the company loses the benefit of a close relationship with their customers. When issues and questions come forward on the Page a company owns and controls, at least there’s the possibility of being able to respond, correct, or connect with the commenters. It’s much harder to take such positive actions on comments posted on any of the thousands of possible venues across the social web.

Best practice for pharma

Understanding that any pharma company has to decide how much risk it can take with the FDA — which hasn’t yet clarified its stance on legal liability of companies in online venues — we recommend companies keep their Facebook Pages open, invest further in them, and provide diligent moderation of comments from the public. (LiveWorld provided relevant comments to the FDA in March of 2010.)

Whether pharma companies do such moderation themselves or outsource to a company like LiveWorld, it’s important to have a program in place, with focused process and attention on off-label use and adverse events. Essentially, that means a connection into the brand’s normal process for reporting adverse events when all parameters for submission are present (identifiable patient, identifiable reporter, specific product involved, and adverse event). Since Facebook doesn’t provide brands with user e-mail addresses, and since brand Pages can’t send private messages to users, this often means responding to a comment that suggests such an event with an address to which the user can write, providing the appropriate information for potential reporting (according to the company’s normal reporting processes). The brand’s Page should also include a clearly-stated process or form for reporting such events.

We also recommend that fully identified, credentialed brand representatives regularly participate on the Facebook Pages, help answer questions, and interact knowledgeably with people — whether discussing valid issues, providing guidance, or correcting misinformation. That way, the company takes and demonstrates full responsibility for the content it provides in its advertising, product-related content, and any articles, blogs, and comments its own people make. And the public gets accurate information, a channel for interaction around questions or concerns, and the opportunity to benefit from the collective experience and input of other brand customers.

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*Facebook Marketing* graphic for LiveWorld series

This post is part of an ongoing “31 Days of Facebook Marketing” series from LiveWorld, a social media agency that offers moderation, insight, and community programming Facebook services for Fortune 1000 brands.

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About the author

Written by

Jenna Woodul is the Chief Community Officer at LiveWorld and co-founder of the company. In her role as executive sponsor and consultant for our clients, Jenna oversees the LiveWorld definition of community culture, strategic planning through community development, and the ongoing evolution of the LiveWorld model as it is propelled by technical innovation and customized to specific client needs. Jenna also tweets from @JennaWoodul. Jenna is based in San Jose, CA.

2 comments to "Getting ready for Facebook pharma changes"

  1. Semantelli

    May 31, 2011

    We don’t think pharma should walk away from facebook, fearing compliance or adverse events(AE) being reported by patients. Industry research shows only 5% of AEs are actually reported through current channels. Having patients report AEs via facebook, and encouraging feedback from patients and doctors on products will help improve patient outcome. We help pharma companies monitor AEs in Facebook with our platform. Facebook isn’t going away and that’s where Gen Y and – you name it Gen – are going to “live”.Siva NadarajahVP, Product Development and StrategySemantelli Corp.http://www.semantelli.com/pharma

    • Jenna

      June 1, 2011

      Thanks for chiming in, Siva. We’ve also seen studies suggesting a flood of AEs should not be feared. So much more to gain, really.

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