Pfizer-BioNTech says vaccine documents hacked in Europe Cyberattack

Two pharmaceutical companies in line for first conditional approval for their Covid-19 vaccine by the EU's medicine regulator said Wednesday their documents were "unlawfully accessed" during a cyberattack on a European Medicines Agency server, reports AFP.

Pfizer and BioNTech said documents relating to their vaccine candidate had been accessed, but that "no systems have been breached in connection with this incident."

"We are unaware of any personal data being accessed," Pfizer said in a statement, while BioNTech said it was "unaware that any study participants have been identified through the data being accessed."

"The EMA has assured us that the cyberattack will have no impact on the timeline for its review," the two companies added.

Meanwhile, Britain's cyber watchdog said it was "working with international partners to understand the impact of this incident affecting the EU's medicine regulator."

"There is currently no evidence to suggest that the UK's medicine regulator had been affected," the National Cyber Security Centre said in a statement.

Britain on Tuesday started rolling out the first vaccine jabs in the Western world of Pfizer and BioNTech's vaccine.

"Swift investigation"

The EU's medicines regulator earlier Wednesday said it had been the victim of a cyberattack, just weeks before it is due to decide on special approval for two coronavirus vaccines.

The Amsterdam-based EMA said the incident was being investigated, but did not specify when it took place or whether its work on Covid-19 was targeted.

"EMA has been the subject of a cyberattack. The agency has swiftly launched a full investigation, in close cooperation with law enforcement and other relevant entities," the EMA said in a brief statement.

An EMA spokeswoman later told AFP "the EMA is fully functional and all work continues".

The Dutch national police high-tech crime team was involved in the probe into the cyberattack, but police gave no more information, the Dutch news agency ANP reported.

The EMA's role as the drugs regulator for the 27-nation EU means it has access to data on the safety and quality of medicines from clinical trials and lab tests from companies that apply for authorisation.

The agency has said it will give a decision on conditional approval for Pfizer-BioNTech's Covid-19 vaccine at a meeting that will be held by December 29 at the latest, while a ruling on Moderna's version should follow by January 12.