The following Studies are available for registration. Choose your study, click on it and follow the process. DALLAS STUDIES: Study #C10-D084: CALLUS CUSHION Start Date: Mar 24 2010 7:30AM End Date: Apr 8 2010 10:00AM Study Description: This study involves 3 Consecutive Clinic Visits During a 1-Week Timeframe. Compensation up to $50.00 (checks to be mailed upon completion of study) GROUP 1: 03/24/10 - 03/26/10 GROUP 2: 03/29/10 - 03/31/10 GROUP 3: 04/08/10 - 04/08/10 Study Objective: This study is being conducted to compare the adherence properties of a callus remover cushion product when used over a wear period of 48 hours. Eligibility: Subjects must be generally healthy males and females age 18 or older. Subjects must be willing to wear the same pair of either dress, work or casual shoes for the 48 hour test period (no athletic shoes will be allowed). Subjects must be willing to bring shoes that have a heel height of ¡Ü1.5 inches and that do not have open shoe areas (e.g., toe, heel or sides)to visit 1. Must be able to read and understand English. 6. Subjects must be willing to wear the assigned cushions for a minimum of 48 hours. Ages: 18 years or older >> View the Study Calendar and Requirements Study #C10-D086: LOOSE POWDER Start Date: Mar 23 2010 3:30PM End Date: May 5 2010 6:30PM Study Description: This Study Involves 3 Clinic Visits over a 6-Week Period. Compensation up to $90.00 GROUP 1: 03/23/10 - 05/04/10 GROUP 2: 03/24/10 - 05/05/10 Study Objective: This clinical study is being conducted in order to determine the safety, acnegenicity and comedogenicity testing of a loose powder. Eligibility: Females age 18-45 years old in general good health. Subjects will have self perceived acne-prone facial skin and/or sensitive skin. Must be able to read & understand English. Ages: 18-45 >> View the Study Calendar and Requirements Study #C10-D058: SPF LOTION Start Date: Mar 22 2010 10:00AM End Date: May 21 2010 1:00PM Study Description: This study involves 4 Clinic Visits over an 8-Week period. Compensation up to $130.00 GROUP 2: 03/22/10 - 05/17/10 GROUP 3: 03/25/10 - 05/20/10 GROUP 4: 03/26/10 - 05/21/10 Study Objective: This clinical study is being conducted in order to evaluate the effectiveness and tolerability of a SPF lotion alone and SPF lotion combined with night cream on female subjects with mild to moderate lines and wrinkles in the periocular area, wrinkles on the forehead area, and nasolabial fold. Eligibility: Females, ages 40 to 65 years of age, inclusive, who are in general good health. Clinically determined mild to moderate fine lines and wrinkles. Potential subjects will be instructed to discontinue the use of facial moisturizers at least 48-72 hours prior to the baseline visit. Must be able to read and understand English. Ages: 40-65 >> View the Study Calendar and Requirements Study #C10-D076: PHOTOAGING Start Date: Mar 19 2010 3:30PM End Date: May 18 2010 6:30PM Study Description: This study involves 4 Clinic Visits over an 8-Week period. Compensation up $130.00 GROUP 2: 03/19/10 - 05/13/10 GROUP 3: 03/23/10 - 05/18/10 Study Objective: This clinical study is being conducted in order to evaluate the effectiveness and tolerability of a hand and body cream on female subjects with moderate photdamaged skin on the hands, neck and chest areas. Eligibility: Females, ages 35-60 years of age, who are in general good health. Clinically determined moderate photodamaged skin on the backs of hands, neck and decolletage. Must be able to read and understand English. Ages: 35-60 >> View the Study Calendar and Requirements Study #C10-D057: FACIAL LOTION Start Date: Feb 25 2010 3:30PM End Date: Apr 27 2010 6:30PM Study Description: This Study Is A Facial Lotion Usage Study Requiring 4 Clinic Visits Over An 8 Week Timeframe. Compensation Up To $130.00 Study Objective: This Clinical Study Is Being Conducted In Order To Evaluate The Effectiveness And Tolerability Of A Face Lotion On Female Subjects. Eligibility: Females In General Good Health, Must Be Able To Read & Understand English. Ages: 40 - 65 Years Of Age >> View the Study Calendar and Requirements Study #C09-D304: ACNE Start Date: Feb 4 2010 3:30PM End Date: Jun 17 2010 6:30PM Study Description: This Study Requires 7 Clinic Visits Over a 12-Week Period. Compensation Up To $300.00 Group 2: 02/04/10-04/29/10 Group 3: 02/23/10-05/18/10 Group 4: 03/09/10-06/01/10 Group 5: 03/15/10-06/07/10 Group 6: 03/25/10-06/17/10 Study Objective: The primary objective is to evaluate the safety, tolerance and efficacy of topical acne treatments. Eligibility: (Screening) Potential subjects will report to the clinic (having removed all facial makeup at least 1 hour prior to their schedule appt) to have their faces examined for the presence of moderate to severe acne. Subjects will need to have between 20 and 50 inflammatory (red, raised) acne lesions, and between 30 and 100 non-inflammatory lesions. Qualified subjects will complete normal paperwork, females (of child bearing potential) will take a pregnancy test. Ages: Male & Females ages 12-45 >> View the Study Calendar and Requirements COLORADO SPRINGS STUDIES: Study #C10-C023 part A and C: Anti-Aging Usage Start Date: Sep 7 2010 11:00AM End Date: Nov 30 2010 6:00PM Study Description: Up to 7 visits over approximately 13 weeks. Visit times vary. Compensation up to $180 for part A and up to $400 for part C. Up to $690 for all three parts. See C10-C023 B for part be details. Study Objective: This 12-week, three-part (A, B and C) clinical research study is being conducted in order to evaluate the effects of a facial product on the skin when used by women with clinically determined facial aging and photoaging skin. Eligibility: Eligible subjects are females ages 35-65, with clinically determined facial aging and photo aging AND self-perceived sensitive facial skin.Cannot be on any other facial, exclusive or usage study. No permanent makeup. Must have a 30-day rest period from any previous facial usage study or study where a test product was applied to the face. All subjects MUST be willing to have 2-mm punch biopsies taken on each crow’s feet area at visit 2 and visit 7 (total of 4 biopsies), if selected. Some scarring may be visible as a result of the biopsies. Subjects selected for biopsies must be willing to return 5-7 days after biopsies for stitch removal. Any subject who qualifies for part A (usage) may participate in parts B and/or C if selected by the clinic. Subjects may NOT be enrolled for part B or part C only. All subjects MUST be available for the dansyl portion of the study. Selected subjects for this portion of the study must agree to NOT use any exfoliating products/devices (chemical, abrasive or manual, such as cleansers, scrubs, sponges, pads, washcloths and/or loofas) on the inner forearms during part C of the study. Must eb willing to follow study guidelines. Ages: 35-65 >> View the Study Calendar and Requirements Study #C10-C211: Stretch Marks Usage Start Date: Aug 27 2010 10:00AM End Date: Dec 1 2010 1:00PM Study Description: 5 visits over approximately 12 weeks. Compensation up to $200. Visit times vary by group. Study Objective: This controlled 12-week usage study is being performed to evaluate the safety (tolerance) and efficacy of a topical cream when used by subjects with stretch marks on their abdomens, hips and/or upper thighs. Eligibility: Eligible subjects are caucasian females, ages 21-40. CANNOT be on any USAGE studies. Cannot have participated in a clinical study involving the lower abdomen, hips, groin area, buttocks or thighs within 2 weeks prior to the study start.CANNOT be on any USAGE studies. Cannot have participated in a clinical study involving the lower abdomen, hips, groin area, buttocks or thighs within 2 weeks prior to the study start. Ages: 21-40 >> View the Study Calendar and Requirements Study #C10-C176: 48 hr patch Start Date: Aug 25 2010 12:00PM End Date: Aug 28 2010 12:00PM Study Description: 3 visits over approximately 3 days. Visit times are 12-1pm for visits 1 & 2, 11am-12pm for visit 3. Compensation up to $60. Study Objective: This study is being conducted in order to assess the potential of test materials to produce skin irritation under controlled conditions. Eligibility: Eligible subjects are males and females, 18-70 years of age. Must have had a two-week rest period from any previous patch test or test where a test product was applied to the back. Cannot have active/history of psoriasis, active allergic skin responses or active eczema anywhere on the body. History of eczema is acceptable. Cannot be participating on any other studies with S7A and/or other facilities. Must be willing to follow study guidelines. Ages: 18-70 >> View the Study Calendar and Requirements Study #C10-C185 (stagger): Facial usage Start Date: Aug 21 2010 9:00AM End Date: Sep 18 2010 10:30AM Study Description: 3 visits over approximately 4 weeks. visi times are 9-10:30 am. Compensation up to $80. Study Objective: This clinical usage study is being conducted in order to evaluate the safety (tolerance) and efficacy of a facial cleanser, moisturizer SPF 15 and baked eye color (one of three eye colors Silver, Lagoon, and Violet Sky) for normal to combination skin type. Eligibility: Eligible subjects are females 18-65 years of age, with self-perceived normal to combination facial skin, who normally wear eye make-up (minimally: eye shadow and waterproof mascara). Females 18-65 years of age, Fitzpatrick I-IV only with self-perceived normal to combination facial skin, who normally wear eye make-up (minimally: eye shadow and waterproof mascara). No known or confirmed allergies to cosmetic products, cleansers, lotions sunscreens or their components. Must be willing to follow study guidelines. Ages: 18-65 >> View the Study Calendar and Requirements Study #C10-C186 stagger: Facial Usage Start Date: Aug 21 2010 9:00AM End Date: Sep 18 2010 10:30AM Study Description: 3 visits over approximately 4 weeks. Visit times are 9-10:30am. Compensation up to $80. Study Objective: This clinical usage study is being conducted in order to evaluate the safety (tolerance) and efficacy of an eye makeup remover and daily face product SPF 40 Eligibility: Females 18-65 years of age, Fitzpatrick I-IV only who normally wear eye make-up (minimally long-wearing eye make-up and/or waterproof mascara). No known or confirmed allergies to cosmetic products, cleansers, lotions sunscreens or their components. Must be willing to follow study guidelines. Ages: 18-65 >> View the Study Calendar and Requirements