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 For Release: Immediately

Pulmo BioTech Announces Details of its Regulatory Approval Experiments

NEW YORK, April 24, 2008. Pulmo BioTech Inc. (OTCBB: PLMO) announced today that its
PulmoScience subsidiary has released details of the areas that it will be investigating as part of the
Regulatory Approval Experiments for Human Trials. The areas are:
- Efficacy Binding Studies
- Characterization of Drug Product Impurities
- Sterility Studies
- Pyrogenicity
- Immunological Testing
- Dosimetry
- Toxicity
PulmoScience will be completing all the relevant tests in each area and seeking Regulatory sign-off
before starting the detailed Human Trials. This is currently expected to be achieved in the first half of
2008.

About Pulmo BioTech Inc.
Pulmo BioTech Inc. specializes in the development and marketing of medical technology and
research. Our proven strengths combine extensive commercial experience and academic
credentials. The principal staff members are acknowledged experts in their specialized field, and
work with a broad range of investment institutions. Pulmo BioTech's mission is to utilize scientific
imagination and drive, together with managerial and financial acumen, to bring innovative and
profitable products to the marketplace to the benefit of all stock holders.

About PulmoScience Inc.
PulmoScience Inc. was established in 2006 , and is currently developing a non-invasive Molecular
Imaging technique for the diagnosis of Pulmonary Embolism, Pulmonary Hypertension and Lung
Inflammatory diseases under the trade name PulmoBind

The company was conceived within the Montreal Heart Institute "MHI" (a world renowned hospital and
educational facility). Jointly owned by MHI subsidiary Innovacor as the technical and operational
partner, Dr Jocelyn Dupuis (the scientific director and originator of the PulmoBind Molecular Imaging
technology), and by Pulmo BioTech Inc as the funding partner, PulmoScience Inc aims to develop this
unique and exciting technology, to fund necessary trials, and to bring the products to market.

PulmoScience believes that the market for its product candidates is worth in excess of $500 million
4 of 4 per annum and that, provided Regulatory Approval is achieved, the safety and efficacy of its products
could allow it to dominate that market.

About PulmoBind
PulmoBind uses an intravenously delivered radionuclide tagged molecule which specifically bonds to
the inner walls of the circulatory system in the lungs, and by the use of an external Gamma Camera
allows an image of the integrity of the blood vessels throughout the lungs to be seen by a diagnostic
clinician. PulmoScience is currently undertaking Regulatory Approval for Phase I Human Trials, and
while subsequent results from additional tests might not corroborate the current results,
PulmoScience believes that PulmoBind has the potential to dominate the market for the diagnosis of
Pulmonary Embolism. In particular, this belief is driven by PulmoScience's expectations of the
improved safety and efficacy that PulmoBind will offer when compared to the current incumbent
nuclear medicine based technology for the diagnosis of Pulmonary Embolism. In addition, early
indications are that PulmoBind could be highly effective in the early stage diagnosis of Pulmonary
Hypertension, a condition for which there is no current front line diagnostic test. The addressable
market for the product candidates being developed by PulmoScience is believed by the company to
be worth in excess of $500 million per annum.

Forward-Looking Statements:
Forward-looking statements contained in this and other written and oral reports are made based on
known events and circumstances at the time of release, and as such, are subject in the future to
unforeseen uncertainties and risks. All statements regarding future performance, earnings
projections, regulatory approval, events or developments are forward-looking statements. It is
possible that the future performance and of the company may differ materially from current
expectations, depending on economic conditions and the uncertainty of regulatory approval. A
change in economic conditions may have a particularly volatile effect on results. Among the other
factors which may affect future performance are: competitive market conditions and resulting effects
on sales and pricing; increases in raw-material costs that cannot be recovered in product pricing; and
global economic factors, including difficulties entering new markets and general economic conditions
such as inflation, interest rates and credit availability. The company makes these statements as of the
date of this disclosure, and undertakes no obligation to update them.

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