Eversheds LLP Richard Lewis United
KingdomMay 24 2012. There has been a steady stream of cross-border life
sciences transactions so far this year such as GSK’s offer for Human Genome
Sciences and Abcam’s acquisition of Epitomics International, both in the US .
Although this year we have seen very few of the mega-mergers of recent years,
last year there was an increase in the number and value of pharma/biotech
M&A transactions, especially in the mid-market $100 million to $1 billion
range.There are a variety of reasons for this but many acquisitions are still
implemented to address the ongoing patent cliff with companies continuing the
search for new drug developments to replace those coming off patent - a recent
example being AstraZeneca’s $1 billion offer for Ardea Biosciences including
its lead product lesinurad in Phase III development for gout. Interestingly,
AstraZeneca’s offer follows closely behind Takeda’s acquisition of URL Pharma
and its branded version of the gout treatment colchicine – highlighting another
reason to acquire, namely where there is a growing market for drugs to combat a
particular disease or where there is an unmet clinical need to tackle a particular
disease.Other reasons we frequently see for acquisitions include those
companies looking for cost synergies, those seeking access to emerging markets
and those looking to access new areas (such as biologics, companion
diagnostics, clinical trial technologies and so on). There is also the ongoing
march of consolidation within the generics and biosimilars market (Watson
Pharmaceuticals’ acquisition of Actavis being a recent example) as well as
originators adding generic capabilities to their product portfolio.Therefore it
seemed like a good time to highlight our top ten issues to be considered in an
M&A transaction.1. Deal structuring: it may seem obvious but at the outset
the parties should ensure that there is a degree of certainty on the key terms
of any transaction - this will reduce a lot of angst further down the line.2.
Cultural awareness: on a cross-border deal, understand at the outset the
cultural complexities involved at the negotiating table and how this might
impact on decision making – this can help manage expectations in advance of and
at negotiating meetings.
3. Buy side execution risk: for sellers it is particularly important to
understand what the key execution risks are for any particular buyer. Typical
concerns relate to buyer specific competition concerns and export control
issues.4. Ability to pay: is the buyer able to pay the purchase price
(including any post closing adjustments, licensing or milestone payments) and
any payments due under any transitional or ongoing arrangements. Sellers should
consider whether to undertake any due diligence (esp financial) on a buyer.5.
Standing behind claims: conversely, for buyers one key issue is understanding
whether cash will be available within the seller post-closing in order to fund
any warranty or indemnity claims post closing. If there are concerns then a
hold-back or escrow arrangement should be considered.6. Due diligence: key
operational areas for consideration include: Commercial contracts – understand what
R&D, clinical trial (and related informed consent), manufacturing, supply,
procurement, outsourcing and pharmacovigilance agreements are in place and any
associated liabilities under those agreements; IP/Patents - the technology licensing and
partnering arrangements of a company (whether in or out) will be key but
equally so, a buyer needs to ensure that it is getting all the rights which it
expects to receive in relation to both patent and trade mark protection (and
understanding any opposition proceedings at European and national offices); Regulatory issues – understand the regulatory
approvals in place whether in Europe, the US or elsewhere, together with the
status of any applications to relevant regulators. Depending on the structure
of the transaction, dossier acquisition and marketing authorisation transfers
may also need to be factored into the timetable; Data protection/privacy – reviews should be
undertaken on data protection compliance and understanding the implementation
program in place; Compliance – spend
time with management to understand what procedures are in place to ensure
compliance with the UK’s Bribery Act and the US Foreign Corrupt Practices Act
(and other similar local legislation); and Product liability – specialist input is often
required to understand the nature of any ongoing product liability disputes,
the likelihood of successful claims and the amount of any liability.Many buyers
address legal due diligence through the data room but there is a lot to be
gained by buyers seeking to have a legal Q&A session as well in order to
understand the commercial context and importance of the various documents.7.
Pricing provisions: ensure that the pricing mechanism is adequately reflected
in the drafting and is appropriate for the basis of valuation, particularly where
“locked box” mechanisms, net asset and working capital adjustments, earn-out
provisions, or milestone payments are included.8. Protection package: the
protection package around the warranties and indemnities and the associated
limitations by which the seller will seek to reduce or limit its liability
typically takes up a lot of negotiating time. Ensure that appropriate legal
specialists are involved who have industry knowledge. Watch out for the use of
a material adverse change clause to enable pre-closing termination of an
agreement in the event of specified market or business events – US buyers in
particular will see this as an important part of the protection package.9.
Leave sufficient time for ancillary documents: there is often a raft of
documents to be negotiated at the same time as the acquisition agreement.
Associated supply and manufacturing agreements will often go right to the heart
of the viability of any price which has been negotiated for the acquisition.
Consider disentanglement carefully where there is a disposal from a group.10.
Integration: finally, consider what arrangements there are for integration
postclosing. The need for specific integration teams depends on the complexity
of the business being acquired. We are currently undertaking some research on
the efficiency of the legal integration process post-closing and more details
on this will be provided later this year.
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