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Investigator Registration
MakroCare's Investigator Registry is a great source for us to identify and qualify appropriate physician investigators for clinical projects.
MakroCare offers following benefits to Investigators for registering :
Appropriate matching of potential clinical trials
Notification of new investigator services
Periodic Newsletters
Personal
Salutation
--Select--
Dr.
Mr.
Mrs.
Ms.
Prof.
Other
First name
Last name
Middle name
Degree
--Select--
M.D.
Ph.D.
Pharm.D.
D.O.
R.N.
Other
Company/ Institute/
Practice name
Division/Department
Contact information
Address1
Address2
Town/City
Country
---Select---
Abkhazia
Afghanistan
Akrotiri and Dhekelia
Åland
Albania
Algeria
American Samoa
Andorra
Angola
Anguilla
Antigua and Barbuda
Argentina
Armenia
Aruba
Ascension Island
Australia
Austria
Azerbaijan
Bahamas
Bahrain
Bangladesh
Barbados
Belarus
Belgium
Belize
Benin
Bermuda
Bhutan
Bolivia
Bosnia and Herzegovina
Botswana
Brazil
Brunei
Bulgaria
Burkina Faso
Burundi
Cambodia
Cameroon
Canada
Cape Verde
Cayman Islands
Central African Republic
Chad
Chile
China
China
Christmas Island
Cocos Islands
Colombia
Comoros
Congo
Congo
Cook Islands
Costa Rica
Côte d'Ivoire
Croatia
Cuba
Cyprus
Czech Republic
Denmark
Djibouti
Dominica
Dominican Republic
East Timor
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Estonia
Ethiopia
Falkland Islands
Faroe Islands
Fiji
Finland
France
French Polynesia
Gabon
Gambia
Georgia
Germany
Ghana
Gibraltar
Greece
Greenland
Grenada
Guam
Guatemala
Guernsey
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
Hong Kong
Hungary
Iceland
India
Indonesia
Iran
Iraq
Ireland
Isle of Man
Israel
Italy
Jamaica
Japan
Jersey
Jordan
Kazakhstan
Kenya
Kiribati
Korea, North
Korea, South
Kosovo
Kuwait
Kyrgyzstan
Laos
Latvia
Lebanon
Lesotho
Liberia
Libya
Liechtenstein
Lithuania
Luxembourg
Macao
Macedonia
Madagascar
Malawi
Malaysia
Maldives
Mali
Malta
Marshall Islands
Mauritania
Mauritius
Mayotte
Mexico
Micronesia
Moldova
Monaco
Mongolia
Montenegro
Montserrat
Morocco
Mozambique
Myanmar
Nagorno-Karabakh
Namibia
Nauru
Nepal
Netherlands
Netherlands Antilles
New Caledonia
New Zealand
Nicaragua
Niger
Nigeria
Niue
Norfolk Island
Northern Cyprus
Northern Mariana Islands
Norway
Oman
Pakistan
Palau
Palestine
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Pitcairn Islands
Poland
Portugal
Puerto Rico
Qatar
Romania
Russia
Rwanda
Saint Barthélemy
Saint Helena
Saint Kitts and Nevis
Saint Lucia
Saint Martin
Saint Pierre and Miquelon
Saint Vincent and the Grenadines
Samoa
San Marino
São Tomé and Príncipe
Saudi Arabia
Senegal
Serbia
Seychelles
Sierra Leone
Singapore
Slovakia
Slovenia
Solomon Islands
Somalia
Somaliland
South Africa
South Ossetia
Spain
Sri Lanka
Sudan
Suriname
Svalbard
Swaziland
Sweden
Switzerland
Syria
Tajikistan
Tanzania
Thailand
Togo
Tokelau
Tonga
Transnistria
Trinidad and Tobago
Tristan da Cunha
Tunisia
Turkey
Turkmenistan
Turks and Caicos Islands
Tuvalu
Uganda
Ukraine
United Arab Emirates
United Kingdom
United States
Uruguay
Uzbekistan
Vanuatu
Vatican City
Venezuela
Vietnam
Virgin Islands, British
Virgin Islands, United States
Wallis and Futuna
Western Sahara
Yemen
Zambia
Zimbabwe
State
Zip code
Phone
Fax
Cell phone
Email address
Web site address
Site Contact Information
First name
Last name
Phone
Fax
Email Address
Function
---Select---
Director
Assistant
Secretary
SMO
Administrator
Study Co-ordinator
Research Narse
Other
Therapeutic Area
1. Primary Therapeutic Area
--Select--
Specialty/Sub-Specialty
--Select--
Research Experience
--Select--
Yes
No
2. Primary Therapeutic Area
--Select--
Specialty/Sub-Specialty
--Select--
Research Experience
--Select--
Yes
No
3. Primary Therapeutic Area
--Select--
Specialty/Sub-Specialty
--Select--
Research Experience
--Select--
Yes
No
Clinical Research Experience
Previous Clinical Research Experience
Pharmaceutical Drug/Compound
Vaccine
Gene-based Therapies
Radiologic
Medical Device
Pharmacokinetics
Diagnostic
Genetics
Current Research/Practice Setting
Phase I Unit
Hospital Outpatient Care
Nursing Home
General Practice
Private Hospital
Public Hospital
Research Center
University Hospital
VA/Military Hospital/Clinic
SMO
Age groups you treat
Neonatology
Pediatric
Adolescent
Adult
Geriatric
Ethics Committee/ Institutional Review Board
Central
Local
Research Experience
Research Phase Experience
Phase I
Phase II
Phase III
Phase IV
Site Capabilities
-70 Freezer
-20 Freezer
Centrifuge
On-Site Lab
On-Site Pharmacy
Home Health
Ultrasound
X-Ray
ECG
Dexa Scanner
CT Scanner
Have you been audited by any of the following?
Makro
FDA
Other Sponsors
Other CROs
Do you have a computerized patient database?
Yes
No
Do you have any previous experience with Makro?
Clinical Trial Monitoring
Interactive Voice Response System
Laboratory Services
Phase IV Periapproval
Past Experience
Compound/Drug Class
Year
Disease State
Phase
I
II
III
IV
Setting
Inpatient
Outpatient
Placebo Controlled?
Yes
No
No. Of Patients Screened
No. Of Patients Enrolled
Enrollment Period From:
To:
Study Conducted by
Makro
Academe
Pharma
Other CRO
Miscellaneous
Do you have Internet access at work?
Yes
No
Do you have experience in conducting studies using Electronic Data Capture (EDC)?
Yes
No
Would you be interested in participating in studies using EDC?
Yes
No
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