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Typed Signatures: Are They Legally Binding?

  • by Zener Engineering Services Ltd
  • 28 Feb, 2025

Life Science Supplier Quote "Typed Signatures Are Industry Standard"

Electronic Signature Electronic Records
In today’s digital world, electronic signatures have become a common method of signing contracts, agreements, validation documents and other important documents in Life Sciences. However, a critical distinction must be made between legally recognised electronic signatures and simple typed 'signatures'. Many individuals and Life Science Organisations assume that typing a name at the bottom of an email or a document equates to a legally binding signature, but this is not the case. Typed signatures are considered by most as not being legally binding in the majority of circumstances and are not considered an industry standard in legal, financial, business transactions or even Life Sciences.

This article explores why typed signatures lack legal validity and therefore should be unacceptable in certainly Life Sciences and Healthcare, and the risks associated with their use. Zener Engineering Services Ltd decided to write this Blog following the above quote being made during a recent visit to a Life Science establishment.

Understanding Typed Signatures

A typed signature is simply a name entered in a document, email, or form using a keyboard. While it may provide a level of personal identification, it lacks critical security measures that legally binding electronic signatures possess. Unlike digital or electronic signatures, a typed name can be easily forged, edited, or manipulated, making it unreliable for authentication purposes.

Electronic signatures (or e-signatures), as defined by laws such as the U.S. Electronic Signatures in Global and National Commerce Act (ESIGN Act) and the European Union’s eIDAS Regulation, must meet certain criteria to be legally binding. These include:

  • Identification and Intent: The signature must be linked to a specific individual with their consent to sign. “Electronic Signature” – The term “electronic signature” means an electronic sound, symbol, or process, attached to or logically associated with a contract or other record and executed or adopted by a person with the intent to sign the record.
  • Security and Authentication: The signature should be protected against tampering and must be verifiable. An advanced electronic signature shall meet the following requirements: (a) it is uniquely linked to the signatory; (b) it is capable of identifying the signatory; (c) it is created using electronic signature creation data that the signatory can, with a high level of confidence, use under his sole control; and (d) it is linked to the data signed therewith in such a way that any subsequent change in the data is detectable.
  • Audit Trail: A legally binding electronic signature system generates logs or records that verify who signed the document and when.

Since a simple typed signature does not meet the above criteria, it is not considered legally binding in most jurisdictions.

For example typed: Name: "FRED BLOGGS" Signature: "fred bloggs"

The Legal Standing Of Typed Signatures

United States

In the U.S., the ESIGN Act signed into law in 2000, provides a general rule of validity for electronic signatures, and the Uniform Electronic Transactions Act (UETA)published by the Uniform Law Commission in 1999. Under these laws, for an electronic signature to be legally binding, it must demonstrate clear intent, consent, and reliability. Merely typing a name into a document or email does not meet these standards because it lacks authentication and proof of intent. 

Courts have consistently ruled against typed signatures in legal disputes due to their vulnerability to fraud, in many cases around the world. For instance, in legal cases where parties attempted to enforce contracts signed with only a typed name, courts often ruled that such signatures did not constitute legally binding agreements. 

A typed signature lacks the security features of a proper e-signature platform, such as multi-factor authentication or a digital certificate, making it easy for parties to deny responsibility.

European Union

The eIDAS Regulation (EU No. 910/2014) sets strict requirements for electronic signatures across the European Union. It classifies electronic signatures as follows:
  • Advanced Electronic Signature (AES) – Requires identity verification and security measures. An advanced electronic signature shall meet the following requirements: (a) it is uniquely linked to the signatory; (b) it is capable of identifying the signatory; (c) it is created using electronic signature creation data that the signatory can, with a high level of confidence, use under his sole control; and (d) it is linked to the data signed therewith in such a way that any subsequent change in the data is detectable.
  • Qualified Electronic Signature (QES) – The highest level, equivalent to handwritten signatures, legally binding across all EU member states. However, it is for national law to define the legal effect of electronic signatures, except for the requirements provided for in this Regulation according to which a qualified electronic signature should have the equivalent legal effect of a handwritten signature.

A typed signature does not fall into either category, which does not hold legal weight unless additional measures, such as authentication or encryption, are in place.

United Kingdom

In the UK, electronic signatures are legally recognised under several legislative frameworks. The primary legislation includes the Electronic Communications Act 2000 and the UK's adoption of the Electronic Identification, Authentication, and Trust Services (eIDAS) Regulation through the Electronic Identification and Trust Services for Electronic Transactions Regulations 2016. These laws establish the validity of electronic signatures, provided certain conditions are met.

Types of Electronic Signatures Recognised in the UK:

  • Simple Electronic Signatures (SES): This category encompasses basic forms of electronic signatures, such as a typed name, a scanned handwritten signature, or clicking an "I agree" button. While SES are legally valid for many everyday agreements, their enforceability can depend on the context and the ability to demonstrate the signer's intent and the signature's authenticity.
  • Advanced Electronic Signatures (AES): AES are uniquely linked to the signer, capable of identifying the signer, created using means under the signer's sole control, and linked to the data in such a manner that any subsequent change is detectable. These features provide a higher level of security and are suitable for more sensitive transactions.
  • Qualified Electronic Signatures (QES): QES meet the highest standard, requiring a qualified certificate issued by a trusted service provider. They are equivalent to handwritten signatures in legal terms and are presumed to be authentic, offering the highest level of assurance.

The Law Commission of England and Wales have confirmed that electronic signatures can be used to execute documents, including where there is a statutory requirement for a signature. This confirmation underscores that, in most cases, electronic signatures serve as a viable alternative to handwritten ones.

Why Typed Signatures Are Not An Industry Standard

Typed signatures do not provide the necessary security measures, which is why Life Science organisations should utilise electronic signature platforms such as DocuSign, Adobe Sign, and HelloSign.

Life Science documents such as validation documentation and test reports require strong authentication which a typed name by an engineer simply cannot provide. In the view of ZES, Life Science documents must be signed using legally valid electronic or handwritten signatures.

A typed signature lacks an audit trail and can easily be altered or forged. In legal disputes, a typed signature does not provide sufficient evidence of agreement, leading to potential contract nullifications. Secure digital signature platforms provide identity verification, timestamps, and encryption. These technologies ensure that documents are enforceable in court, unlike typed names that can be manipulated.

In healthcare, patient consent forms should be signed securely to comply with applicable laws which typed signatures simply do not provide. They do no provide adequate security or proof of consent, which is why electronic signature platforms with authentication features are widely used.

As typed signatures do not meet the security standards required for enforceable agreements, Life Science organisations should utilise digital signature solutions that provide:

  • Verification of the signer’s identity
  • Timestamping and tamper-proofing
  • Legal enforceability in multiple jurisdictions

Risks Of Using Typed Signatures

Lack Of Security

A typed name can be easily copied and pasted by anyone, leading to fraud and identity theft. Unlike digital signatures, which encrypt data and verify identities, a typed signature has no built-in security.

Non-Enforceability In Court

If a contract or agreement is disputed in court, a typed signature offers little proof of the signer’s intent and identity. This increases the risk of agreements being declared invalid.

Higher Risk of Forgery

As anyone can type another person’s name into a document, typed signatures are therefore highly vulnerable to forgery. This creates potential serious risks for Life Science organisations, their operation, their reputation and ultimately the patient.

Non-Compliance With Industry Regulations

Many industries have strict compliance requirements for signatures, including Life Sciences, so why do Life Science Suppliers think otherwise? Using a typed signature may lead to regulatory violations, fines, or legal disputes.

Alternatives To Typed Signatures

Electronic Signature Platforms

To ensure legal validity and industry compliance, individuals and businesses should consider the use of trusted electronic signature solutions such as:

  • DocuSign
  • Adobe Sign
  • HelloSign
  • SignNow

These platforms provide encryption, identity verification, and audit trails, making them legally binding and industry-approved. A suitable validation exercise should be carried out to ensure your chosen platform actually meets the requirements of the Life Science organisation and applicable laws and regulations.

Digital Signatures

Digital signatures use cryptographic technology to secure documents. Unlike typed signatures, they provide authentication, tamper-proofing, and legal enforceability. Digital signatures are now widely accepted in the Life Science Industry.

Handwritten Signatures

For maximum security in Life Sciences, handwritten signatures remain a strong alternative. When paired with notarization or witnessed signing, they provide a high level of authenticity and legal recognition.

Summary

In summary, whilst in 2025 typed signatures may be convenient, they are not legally binding or an " industry standard". They lack security, authentication, and enforceability in UK and USA courts. In today’s digital age, most large Life Science organisations rely on electronic and digital signature platforms to provide security and legal recognition.

If you are signing important documents such as, Validation Test Reports, Batch Release Reports etc, using a trusted e-signature provider ensures compliance, prevents fraud, and guarantees that your signed documents are enforceable. 

In the view of ZES, typed signatures as in "Name: FRED BLOGS Signature fred bloggs" have no place in the Life Science Industry today!

Avoid typed signatures to protect yourself, your Life Science Organisation but most of all the Patient.

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