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Q1 2018 Update Doug Bryant, President & CEO Randy Steward, CFO RJ Deck Feb 2018

Q1 2018 Update - Seeking Alpha

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Q1 2018 UpdateDoug Bryant, President & CEO

Randy Steward, CFO

RJ Deck Feb 2018

Forward-Looking Statements

2

This presentation contains forward-looking statements within the meaning of the federal securities laws that involve material risks, assumptions and

uncertainties. Many possible events or factors could affect our future financial results and performance, such that our actual results and performance may

differ materially from those that may be described or implied in the forward-looking statements. As such, no forward-looking statement can be guaranteed.

Differences in actual results and performance may arise as a result of a number of factors including, without limitation, fluctuations in our operating results

resulting from seasonality, the timing of the onset, length and severity of cold and flu seasons, government and media attention focused on influenza and the

related potential impact on humans from novel influenza viruses, adverse changes in competitive conditions in domestic and international markets, changes

in sales levels as it relates to the absorption of our fixed costs, lower than anticipated market penetration of our products, the reimbursement system

currently in place and future changes to that system, changes in economic conditions in our domestic and international markets, the quantity of our product

in our distributors’ inventory or distribution channels, changes in the buying patterns of our distributors, and changes in the healthcare market and

consolidation of our customer base; our development and protection of intellectual property; our development of new technologies, products and markets;

our reliance on a limited number of key distributors; our reliance on sales of our influenza diagnostics tests; our ability to manage our growth strategy; our

ability to integrate companies or technologies we have acquired or may acquire, including integration and transition risks, the ability to achieve anticipated

financial results and synergies, and effects of disruptions or threatened disruptions to our relationships, or those of the acquired businesses, with

distributors, suppliers, customers and employees; intellectual property risks, including but not limited to, infringement litigation; our debt service

requirements; our inability to settle conversions of our Convertible Senior Notes in cash; the effect on our operating results from the trigger of the

conditional conversion feature of our Convertible Senior Notes; the possibility that we may incur additional indebtedness; our need for additional funds to

finance our operating needs; volatility and disruption in the global capital and credit markets; acceptance of our products among physicians and other

healthcare providers; competition with other providers of diagnostic products; adverse actions or delays in new product reviews or related to currently-

marketed products by the FDA or any loss of previously received regulatory approvals or clearances; changes in government policies; compliance with

other government regulations, such as safe working conditions, manufacturing practices, environmental protection, fire hazard and disposal of hazardous

substances; third-party reimbursement policies; our ability to meet demand for our products; interruptions in our supply of raw materials; product defects;

business risks not covered by insurance and exposure to other litigation claims and potential adverse outcomes of such legal proceedings; interruption to our

computer systems; competition for and loss of management and key personnel; international risks, including but not limited to, compliance with product

registration requirements, exposure to currency exchange fluctuations and foreign currency exchange risk sharing arrangements, longer payment cycles,

lower selling prices and greater difficulty in collecting accounts receivable, reduced protection of intellectual property rights, political and economic

instability, taxes, and diversion of lower priced international products into U.S. markets; dilution resulting from future sales of our equity; volatility in our

stock price; provisions in our charter documents, Delaware law and our Convertible Senior Notes that might delay or impede stockholder actions with

respect to business combinations or similar transactions; and our intention of not paying dividends. Forward-looking statements typically are identified by

the use of terms such as “may,” “will,” “should,” “might,” “expect,” “anticipate,” “estimate,” “plan,” “intend,” “goal,” “project,” “strategy,” “future,”

and similar words, although some forward-looking statements are expressed differently. The risks described in reports and registration statements that we

file with the Securities and Exchange Commission (the “SEC”) from time to time, should be carefully considered. You are cautioned not to place undue

reliance on these forward-looking statements, which reflect management’s analysis only as of the date of this presentation. Except as required by law, we

undertake no obligation to publicly release the results of any revision or update of these forward-looking statements, whether as a result of new information,

future events or otherwise.

Our Strategic Intent

3

Build a broader-based diagnostic company that delivers revenue and marginmore consistently. Use existing resources to fortify price and volume in our core

businesses, while using our capabilities to attack the limitations of ourcompetitors, and to forge ahead to create new markets.

Sofia® Immunoassay platform

is the next generation,

objectively-read system in

support of our legacy lateral

flow business, designed to

deliver more value and a

higher gross margin.

Sofia captures market share

with the first wave of assays

(for Respiratory Disease) in

physician offices, hospitals

and alternate sites.

FDA-Cleared, CLIA -Waived

Immunoassay

Sofia® 2, at a fraction of the cost of

the original Sofia,

can further penetrate the lower-

volume and higher-volume

segments of the POC testing

market.

Sofia 2’s integrated wireless options

will expand connectivity with the

potential increase overall diagnostic

testing.

FDA-Cleared, CLIA – Waived

Our Innovative New Products are Designed to Meet the Various Needs of the Customer in Any POC Setting

4

Triage® MeterPro® is our cost effective, easy to use instrument for cardiovascular and toxicology diagnostic assays. Multipleimmunoassays can run on the same platform, with rapid resultsin about 15-20 minutes

The MeterPro instrument can run multiple sample types, such as whole blood, plasma, or urine,with process controls built into the meter, software and test device

FDA-Cleared

Molecular

AmpliVue, a non-

instrumented, hand-held

disposable molecular device

requires no thermocycler or

upfront costs. Moderately

complex claim provides an

easy-to-use entry point into

molecular testing for smaller

hospitals and lower-volume

users wishing to convert from

legacy testing methods.

FDA - Cleared, Mod - Complex

Solana, our first instrumented

molecular system, extends

AmpliVue’s proprietary HDA

technology to offer a low-cost,

medium volume molecular

solution that can multiplex,

running up to 12 samples at a

time in approx. 30 minutes.

Solana is designed for

samples that do not require

extraction or quantitation in

the mod-complex setting.

FDA - Cleared, Mod - Complex

Lyra, our Real-time molecular

PCR assays, are designed to

run on a hospital lab’s existing

thermocycler, and provides a

real-time testing solution to

higher throughput labs using a

hospital’s established systems

– with no upfront costs.

Lyra molecular assays can be

paired with other Lyra assays

to create customized multiplex

Respiratory Disease panels.

FDA - Cleared, Highly - Complex

Savanna is our low-cost, fully

integrated “sample-to-answer”

molecular diagnostic system.

Target cartridge cost is less

than $5 and target instrument

cost is $10,000, designed for

low-volume and potentially

CLIA-waived settings.

Savanna can run either

traditional PCR or HDA

assays for samples that do not

require extraction.

In Development

Our Innovative New Products are Designedto Meet the Various Needs of the Customer in Any POC Setting

5

6

Mod -

Complex

Our R&D and Regulatory expertise is what fuels our growth…

Since 2011, Quidel has submitted over 30 510(k) packages resulting in over 25 FDA clearances and expanded product claims, 5 CLIA - waiver designations and numerous product introductions,

contributing $95M in annual revenues1

Quidel Recent Commercial Initiatives: FDA-cleared Products since 2011

Mod -

Complex

Highly -

Complex

Highly -

Complex

Highly -

Complex

Highly -

Complex

Highly -

Complex

Highly -

Complex

Highly -

Complex

Sofia®

Instrumented Immunoassay

AmpliVue® HDA IsothermalMolecular

Solana® HDA IsothermalMolecular

Lyra® Real-Time PCRMolecular

CLIA -

Waived

CLIA -

Waived

CLIA -

Waived

CLIA -

Waived

Sofia Analyzer

Influenza

A + B

Group A Strep

RSV

hCG

Lyme Disease

Legionella

(CE Mark

only)

Mod -

Complex

Mod -

Complex

Mod -

Complex

Mod -

Complex

C. difficile

Group A Strep

Group B Strep

Pertussis

Mod -

Complex

Mod -

Complex

Trichomonas

HSV 1 + 2

Mod -

Complex

Mod -

Complex

Mod -

Complex

Solana

Instrument

Influenza A + B

Group A Strep

Influenza A + B

RSV + hMPV

Adenovirus

Parainfluenza

123

Strep A + C/G

C. difficile

HSV 1+ 2/VZV

Mod -

ComplexStrep Complete

(A + C/G)

Mod -

ComplexTrichomonas

Mod -

ComplexHSV 1+2/VZV

Sofia 2®

Instrumented Immunoassay

CLIA -

Waived

CLIA -

Waived

Sofia 2

Analyzer

RSV

1. Latest TTM combined revenues for Sofia and Molecular products.

Not all FDA submissions and clearances since 2011 are shown.

Mod -

ComplexRSV + hMPV

CLIA -

WaivedInfluenza A+B

S. Pneumo

(CE Mark

only)

Mod -

ComplexC. difficile

CLIA -

WaivedStrep A+

Mod -

ComplexGroup B Strep

7

Integration Progress Since Day 1

7

IntegrateTransitio

n Assess

Apr 17 Jul 17 Oct 6

October 2017

Transitioned 472 US employees

Successfully implemented US Order-

to-Cash for US and 24 direct export

markets (53% of Revenue): Assumed

US contracts and Sales & Marketing

functions

November 2017

Selected EU Shared Service Center

site in Galway IR; Lease under

negotiation

Deal

Announced Day 1

December 2017 January 2018

Hired 50 commercial employees

across China, Germany, Italy, and

Austria

Completed Sale/Leaseback of

Summers Ridge Facility - $149M

Moved 100% of Employees to Bldg

C&DRestructured North American Sales to

incorporate Triage and BNP products Began Synergy planning

Developed Global Order to Cash

transition plan

8

Building the Quidel Global Footprint

Revenue estimates are FY2016

Geographical Footprint of Combined Business

Note: All revenues correspond to FY ‘16

Canada

$8 M

2%

EMEA

$56 M

12%

52%

Quidel

10%

BC-BNP

38%

Triage

52%

Quidel

23%

BC-BNP

25%

Triage

US

$305 M

66%

39%

Quidel

1%

BC-BNP

61%

Triage

LATAM

$17 M

4%

17%

Quidel

38%

BC-BNP

45%

Triage

China

$50 M

11%

5%

Quidel

36%

BC-BNP

59%

Triage

Asia

$22 M

5%48%

Quidel

11%

BC-BNP

41%

Triage

9

We Now Ship to 150+ Distributors Serving 90+ Countries and Creating Demand in 12 Markets

SAN DIEGO

10

Direct

Shipments

Triage Acquisition Was Transformational for the International Business

Note: All revenues correspond to FY ’16

*Includes sales for ‘Specialty Products’ group

$33M

Quidel

$33 M*

Quidel

Int’l Sales

$77M

Triage

65%

$42M

BC-BNP

35%

$120 M

Triage + BC-

BNP

Int’l Sales

$153 M

Combined

Entity Int’l

Sales

$77M

Triage

50%

$42M

BC-BNP

28%

$33M

Quidel

22%

11

Quidel’s Multiple Near-Term Catalysts will Grow the Non-flu Business.

Category Product

Sofia and Sofia 2

Immunoassays

Sofia/Sofia 2 Strep A

Sofia/Sofia 2 RSV

Sofia Lyme

Sofia Vitamin D

InflammaDry and AdenoPlus for Eye Care Market

Alternate/Adjacent Markets

Bio Assays Graves’ Disease/Hashimoto’s (TBI)

Solana

Molecular

Strep A

C. difficile

GBS, HSV 1+2/VZV, Trichomonas

Research - Bone Health New Bone Health and Renal Markers

Cell Culture Custom Cells

TriageCardiovascular internationally, and through BNP;

Toxicology output via operational improvements

12 Reflects products in development and other anticipated catalysts.

M&A Strategy

13

Use cash on hand to pay down debt and pursue inorganic opportunities to diversify and augment

the non-respiratory part of the business

• Targets range from tuck-ins up to equal size

• New technology that accelerates the advancement of in-house

MDx abilities

• Products that reduce the seasonality, volatility of flu season

• Firms that can leverage our international market presence

• Accretive within 12-24 months

What we’re looking for…

Q&AInvestors ContactRuben ArguetaQuidel CorporationO: 858.646.8023E: [email protected]

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